How much can a buyer actually verify before trusting the product?
Most pet supplement brands ask pet parents to trust polished packaging, science-sounding language, or badges that do not show the underlying proof. This report looks only at what each brand makes public: doses, ingredient rationale, named experts, testing, manufacturing, evidence, and claim discipline. La Petite Labs publishes the report and is scored separately as a Publisher Benchmark, not included in the rankings.
56brands ranked
100public transparency points
8buyer questions answered
Jul 3, 2026report updated
2026 Executive Summary
Trust language is everywhere in pet supplements. Verifiable evidence is rare.
Across the 56 ranked brands, the median public-transparency score was 57.3/100 — the field runs from 87 at the top to 34 at the bottom.
Only seven of 56 ranked brands let a buyer trace a specific lot number to its own lab report before purchase.
Only seven of 56 disclose the manufacturing facility behind their products at the named-facility level.
Three of 56 have published a peer-reviewed clinical trial on a finished formula — the rest rely on ingredient-level research.
23 of 56 use veterinary-credibility language without naming a single veterinarian anywhere a buyer can check.
No ranked brand earned the Public Evidence System award in this review cycle.
If you only do one thing: pick the product you're considering and try to find its per-active doses and its lab report. That two-minute test reproduces most of the spread in this ranking.
How to read our placement: La Petite Labs publishes this report, so it is graded under the same rubric but shown separately as a Publisher Benchmark — never ranked, never eligible for awards.
What stood out
01
Doses matter. Brands that hide actives behind proprietary blends make it harder for buyers to compare formulas or to give pets an informed amount.
02
Testing is not the whole story. A clean COA shows what is or is not in a bottle, but it does not explain why the formula exists.
03
Named experts matter. "Vet-formulated" means less when no veterinarian is named with credentials and scope of involvement.
04
Borrowed science is common. Many brands cite ingredient research as if it proves the finished product. Real finished-formula trials are rare.
05
La Petite Labs does not rank itself. We publish the report, so our score is shown separately as a Publisher Benchmark instead of being mixed into the competitive ranking.
View La Petite Labs roadmap to the 90+ band ↓
Our Publisher Benchmark score is 83.5. The Industry Transparency Standard band begins at 90. The five public-surface commitments below would move La Petite Labs into that band — graded under the same rubric every other brand is held to.
Ship full-line COA-lookup coverage with a published panel scope. Every currently sold SKU resolves to a public, lot-linked COA; pesticide, mycotoxin, allergen, microbial, heavy-metal, and active-potency testing itemized within the published panel.
Surface per-active dose disclosure directly on the bundle PDP. Both component supplement facts panels visible side-by-side at the same page depth as the bundle add-to-cart.
Publish a named per-formula scientific owner for each finished product. Each PDP lists its named scientific owner with credentials, scope (formulated / reviewed / safety-audited), and bio URL.
Consolidate the trust surface into a single Evidence & Trust hub. One landing page consolidates the four evidence pillars (science, testing, named experts, manufacturing) plus the published rubrics.
Publish finished-formula clinical evidence on at least one product in the line. Named institution, named principal investigator, registered trial identifier, pre-registered outcomes, results published regardless of direction.
Progress is reviewed at each annual major-update cycle.
Symbol keyHow to read the badges and watchoutsBrand signals · watchouts
Each ranking row earns badges for what the brand publishes well, and
may carry up to three Worth Noting watchouts for limitations buyers should
be aware of. The same rules apply to every brand on this page, including
La Petite Labs.
Public Evidence System
The brand publishes buyer-verifiable evidence across the main pillars — label disclosure, ingredient rationale, clinical evidence, named experts — at a level a buyer can independently check before purchase.
Flagship
Named Vet Reviewer
The brand surfaces at least one named veterinarian, nutritionist, or scientific advisor with credentials and disclosed scope of involvement (formulator, reviewer, advisor, commentator).
Ingredient Rationale
The brand publishes ingredient-by-ingredient rationale explaining why each meaningful active is in the formula and what biological role it plays.
Disease-Claim-Free
The brand avoids disease-treatment claims, lifespan guarantees, "clinically proven" language without citation, and other consumer-protective language failures across its marketing surface.
Public COA Lookup
The brand publishes a public lookup for Certificates of Analysis (lab reports) so buyers can see test results for actives, contaminants, and microbial purity.
Per-Lot Traceability
Buyers can match a specific bottle or pouch (by lot number) to its own lab report — not just a generic sample COA.
NASC Member
The brand is a current member of the National Animal Supplement Council with active Quality Seal participation.
Finished-Formula Trial
The brand has published a clinical study of the finished formula (not borrowed from an individual ingredient). Distinct from "clinically tested" marketing language.
Named Mfg Facility
The brand discloses its manufacturing facility at the named-facility level (facility name, city, state) with at least one quality-system certification visible.
Worth Noting · watchoutsWatchouts surface honest limitations in a brand's public evidence. Tap any watchout for the institutional meaning.
Closed Science
The brand publishes strong testing or COA evidence but does not surface ingredient rationale, named experts, or finished-formula evidence. Testing alone is not enough to make the science verifiable.
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
Evidence Buried
The brand technically publishes meaningful science, evidence, testing, or expert disclosure, but buyers cannot reach it without dedicated effort. Evidence that exists but is hard to find counts less.
Higher scores reward
Breadth, disclosure, and substantiation.
Brands score high when buyers can independently verify the formula, science, named experts, testing, and claims — without emailing support or trusting marketing language.
Per-active milligram amounts disclosed on the public label.
Named third-party lab, published Certificate of Analysis, lot-level traceability.
Public substantiation for marketing claims — citations, not adjectives.
Lower scores may mean
Narrower scope, or less of the work published.
Brands score lower when evidence is missing, hidden behind support contact, or substituted with vague language ("clinically tested," "veterinarian-formulated," "third-party verified") that cannot be checked.
Actives are listed without per-serving amounts (proprietary blends).
Testing language is vague — no named lab, no public COA, no lot linkage.
Claims outrun the public evidence record at time of review.
A lower score does not automatically mean a product is unsuitable. It may simply
be narrower in scope, less transparent, or supported by fewer public quality
signals than this rubric rewards.
Publisher disclosure · Scored, Not Ranked
La Petite Labs is a brand operated by American Valley LLC, which publishes this report and sells products in this category. LPL is scored under the same rubric but shown separately as a Publisher Benchmark, excluded from the ranking table and awards.
0
Rank
83.5/100
as of 2026-05-23
Strong
PUB
Benchmark
Publisher product
La Petite Labs
American Valley LLC
Publisher of this report
Publisher Brand
83.5/100
as of 2026-05-23
Strong
Publisher of this report and excluded from the ranking and from awards. Graded as a Publisher Benchmark under the same rubric and the same standards as every brand surveyed. Strong on label disclosure (per-active mg across the line), scientific rationale (Science Journal indexing proprietary editorial frameworks), evidence and clinical citation (A-D grading + PK tagging + PubMed citations at ingredient level), named veterinary network (six DVMs with framework authorship and review scope), claim discipline, and overall buyer-accessibility (six trust pages within one click of home). Remaining gaps disclosed in the brief: no published finished-formula clinical trial yet on any LPL product, no named per-formula scientific owner tied to Hollywood Elixir, Pet Gala, or the Pampered System, partial COA-lookup rollout across the line, manufacturing identity disclosed at country level only, no above-the-fold 'not a substitute for veterinary care' qualifier on bundle framing, and no consolidated 'Evidence & Trust' hub landing page.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreePublic COA LookupPer-Lot TraceabilityNASC MemberFinished-Formula TrialNamed Mfg Facility
What's in it
Per-active mg disclosure across every product in the line, with no proprietary blends.
Consolidated Science Journal in primary navigation indexing proprietary editorial frameworks authored by named DVMs (Dr. Pendergrass on the 12 Hallmarks of Aging in Dogs; Dr. Calvin on the Pet Integumentary System; plus Cross-Species Formulation, Single-Nutrient vs Systems, Why Many Pet Supplements Fall Short).
Per-product Research pages cite 8 PubMed-linked peer-reviewed studies with explicit A-D evidence grading and PK1-PK3 pharmacokinetic confidence tagging, separating direct ingredient-level evidence from extrapolated evidence and disclosing that no finished-formula clinical trial has yet been published.
What's not in it
No named in-house lead formulator publicly tied to the specific Hollywood Elixir, Pet Gala, or Pampered System finished formulas — the veterinary network is framed as scientific review, safety auditing, and framework authorship rather than as named product formulators.
Manufacturing location is disclosed only at country level; the NASC Preferred Supplier status belongs to the unnamed contract manufacturer, not La Petite Labs or American Valley LLC.
COA lookup tool exists and is surfaced in primary navigation, but rollout coverage across the product line is still partial — full per-SKU lot-lookup coverage has not yet shipped.
Why this score
itap any criterion for evidence
——
Why this score
What's missing
Brand's own words
Both flagship products (Hollywood Elixir, Pet Gala) and the Pampered System bundle disclose every meaningful active by mg/IU/mcg, with no proprietary blends and clearly defined serving sizes. Hollywood Elixir's current package panel surfaces NR 60 mg, glutathione 50 mg, CoQ10 40 mg, astaxanthin 2 mg, quercetin 25 mg, beta glucans 50 mg, reishi 25 mg, individually dosed B vitamins, and whey protein isolate 250 mg; it does not list taurine. Pet Gala surfaces 13 actives at full mg disclosure. The bundle PDP requires one click into a component PDP to see the full dose panel side-by-side, which is the only structural gap.
Held below 10 because the Pampered System bundle PDP does not yet surface both component dose panels side-by-side on the bundle page itself. Buyers must click into Hollywood Elixir and Pet Gala PDPs individually to compare. A consolidated dose-panel display on the bundle PDP would lift this to 10.
The brand publishes a consolidated Science Journal in primary navigation that indexes multiple proprietary editorial science frameworks authored by named DVMs: The 12 Hallmarks of Aging in Dogs (Dr. JoAnna Pendergrass, DVM), The Pet Integumentary System (Dr. Sarah Calvin, DVM), The Science of Cross-Species Formulation, Why Single-Nutrient Thinking Often Falls Short, Why Many Pet Supplements Fall Short, Nutrition and Drug Approaches in Pet Health, and Skin and Coat Clues to Systemic Disease. Per-product Research pages articulate ingredient selection, biological role, and mechanism at the active level. The Hollywood Elixir Research page surfaces the LPL-01 design framework, Biological Defense Coverage, the trademarked Canine and Feline Gerosciences framework, and an NAD+ Pharmacology Appendix. Mechanism content is real and substantive, not benefit assertion. Held below 10 only because the brand does not yet publish a single 'How LPL Formulas Work' landing page that consolidates every mechanism page in one anchor.
No single consolidated 'How LPL Formulas Work' landing page yet — mechanism content is distributed across the Science Journal index, per-product Research pages, and individual framework pages. Consolidating into one landing page (while preserving the deep pages) would lift to 10.
Rather than stacking ingredients, we construct formulas around mechanism, interaction, and long-term biological effect.
Pilot-evaluator confirmed directly on the Hollywood Elixir Research page: 8 peer-reviewed studies are surfaced with PubMed links and full publication context (Watowich 2024 Scientific Reports; Schmid 2024 GeroScience; Druzhaeva 2021 AJVR; Abreu 2015 IJP; Reinboth 2010 JAFC; Park 2019 Vet. Med.; Kayser 2024 J. Anim. Sci.; Creevy 2022 Nature). The page applies explicit A-D evidence grading and PK1-PK3 pharmacokinetic confidence tagging to distinguish stronger direct evidence from weaker extrapolated evidence. It separates ingredient-level research from finished-formula research. The brand does not borrow unrelated trials and does not use 'clinically tested' or 'clinically proven' language without underlying support. Held at 8 rather than 9 because the A-D + PK grading framework is applied to ingredient-level evidence only, and no published finished-formula clinical trial yet exists on any LPL product. Ingredient-level evidence with grading discipline is not equivalent to finished-formula evidence; the rubric does not award the 9-10 tier without finished-formula RCT or substantively comparable direct evidence.
No published finished-formula clinical trial on any LPL product (disclosed). The A-D + PK1-PK3 grading framework improves evidence legibility by separating direct evidence from extrapolated evidence, but is currently most prominently surfaced on the Hollywood Elixir Research page; extending the same grading discipline visibly to the Pet Gala Research page closes one part of the gap. The 9-10 tier requires a finished-formula RCT or equivalent direct evidence.
It applies explicit evidence grading (A–D) and pharmacokinetic confidence tagging (PK1–PK3) to distinguish what is proven in dogs from what is inferred or theoretical.
The brand identifies six named veterinary contributors, with scopes ranging from framework authorship to expert commentary and review. Surfaced from primary navigation. Dr. Sarah Wooten (DVM, CVJ — UC Davis): veterinary contributor and pet health journalist. Dr. JoAnna Pendergrass (DVM — Virginia-Maryland CVM, Emory postdoc): publicly named author of LPL's 12 Hallmarks of Aging in Dogs framework. Dr. Sarah Calvin (DVM — Washington State): publicly named author of LPL's Pet Integumentary System framework. Dr. Joseph Menicucci, DVM: dedicated public dossier page. Two additional credentialed contributors named: Dr. Joanna Woodnutt (BVM, BVS, MRCVS) and Dr. Crisanto Villarey (DVM). A dedicated Veterinary Professionals hub provides a separate practitioner-facing surface. Scored 8 under the standardized expert ladder: multiple named DVM advisors with framework-level scope, but no named lead formulator or scientific advisor tied specifically to the finished Hollywood Elixir, Pet Gala, or Pampered System formulas. The 9-10 tier requires explicit per-formula scope of ownership (formulated / reviewed / safety-audited / medically reviewed) attached to specific finished products.
No named in-house lead formulator or scientific advisor publicly tied to the specific Hollywood Elixir, Pet Gala, or Pampered System finished formulas. The veterinary network is well-disclosed at the framework-authorship level; the 9-10 tier requires explicit per-formula formulation ownership or safety-review scope attached to specific finished products.
La Petite Labs collaborates with veterinarians and scientists who provide scientific review, safety auditing, and expert commentary on our proprietary frameworks
Pilot-evaluator confirmed directly on the Quality & Testing Standards page: NSF and Eurofins are both named as third-party laboratory partners. The page describes per-batch testing covering heavy metals, microbial contamination, and active-ingredient potency. A dedicated Verify Your COA portal is surfaced from primary navigation with a working lot-number lookup field. Held at 8 (not 9) because the brand discloses on its own COA page that lot-lookup rollout is still in progress — Hollywood Elixir lot-lookup goes live June 2026, Pet Gala completes by end-of-year, Pampered System not yet covered. The COA page itself states 'Some older or transitional batches may not yet be available in the lookup system' — disclosed rollout state rather than over-promise. Score will lift to 9 the moment lot-lookup is live for every currently sold SKU, and to 10 when surfaced directly on each PDP and when the panel scope (pesticides, mycotoxins, allergens) is explicitly itemized.
Coverage across line is currently 'partial' rather than full. Score is held at 8 until lot-lookup is live for every currently sold SKU. The lot-lookup tool is also best surfaced on individual product PDPs (not only on the Quality & Testing Standards page and the dedicated COA portal). Additionally, the Quality & Testing page does not yet explicitly itemize pesticide, mycotoxin, and allergen testing within the third-party panel.
This service is available for Hollywood Elixir® starting June 2026. Pet Gala™ will complete its lookup service roll-out by end-of-year.
Public materials disclose U.S. manufacturing by a contract manufacturer with NASC Preferred Supplier status, plus FDA-registered and cGMP-compliant manufacturing conditions. The NASC Preferred Supplier status belongs to the contract manufacturer, not La Petite Labs or American Valley LLC, so LPL is not awarded the report's brand-level NASC Member signal. Sourcing logic is described in editorial copy. The structural gap is that the contract manufacturer and specific facility name, city, and state are not currently surfaced publicly — manufacturing location is disclosed at country level rather than the named-facility level the rubric rewards at the 10/10 tier.
The contract manufacturer and facility name, city, and state are not surfaced publicly, so buyers cannot connect the disclosed NASC Preferred Supplier status to a named manufacturer record. LPL receives no brand-level NASC Member signal. Naming the manufacturer and facility and linking the manufacturer's exact NASC record would improve buyer verifiability.
Manufactured in a NASC Preferred Supplier facility in the USA under FDA-registered, cGMP-compliant, HACCP-certified conditions.
Brand marketing across home page, PDPs, What-Is pages, and Research pages avoids disease-treatment claims, exaggerated lifespan claims, 'clinically proven' language without citation, and unsupported before/after implications. The brand explicitly discloses that no finished-formula clinical trial currently exists on its products, rather than using clinical-style language to imply otherwise. The 'Why Many Pet Supplements Fall Short' framework and the public Editorial Guidelines page articulate the brand's claim-discipline thesis. Scored at 8 (not 9) because above-the-fold framing on the home page and the bundle PDP uses 'complete daily wellness system' language that, while explained in supporting copy, is not qualified above-the-fold with an inline limit such as 'not a substitute for veterinary care or complete nutrition.' Score lifts to 9 the moment above-the-fold qualifiers are added.
Above-the-fold 'complete' framing on the bundle PDP and home page carries no inline qualifier. Adding 'not a substitute for veterinary care or complete nutrition' (or equivalent) above-the-fold would lift this to 9. Tightening every broad 'wellness system' phrase across major surfaces is the gate to 10.
the finished formula does not yet have a published clinical trial
Primary navigation surfaces six trust pages within one click of the home page: LPL-01 Standard, Science Journal, Veterinary Experts, Quality & Testing Standards, Flavor & Palatability, and Verify Your COA. Each product line additionally exposes dedicated What Is, Research, Quality & Testing, Ingredients, and Benefits pages from its own sub-navigation. The four evidence pillars (science, testing, named experts, manufacturing) are each addressable in one click. Held below 10 only because the brand does not yet consolidate these into a single 'Evidence & Trust' hub landing page — buyers reach evidence quickly, but via multiple top-level links rather than one anchor.
Six trust pages exist in primary nav but are not consolidated into a single Evidence & Trust hub. Building one anchor page that links to Science Journal, Quality & Testing, Verify Your COA, Veterinary Experts, LPL-01 Standard, and the published rubrics would lift this to 10.
evidence-aware pet wellness resources grounded in formulation transparency, species-appropriate safety logic, and the LPL-01 Standard
American Valley LLC · Core Publisher of this report
Publisher of this report and excluded from the ranking and from awards. Graded as a Publisher Benchmark under the same rubric and the same standards as every brand surveyed. Str...
83.5/100
Strong
Every number below is a public transparency score: what a buyer can verify from public materials before purchase — not effectiveness, safety, ingredient quality, or customer satisfaction. Read the full methodology.
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1
Rank
87/100
as of 2026-06-13
Strong
1
Rank
ElleVet Sciences
ElleVet Sciences
South Portland, Maine, United States
87/100
as of 2026-06-13
Strong
ElleVet Sciences sits well above the category median on research and expert disclosure: it cites peer-reviewed finished-formula trials with authors and journals, names a credentialed CMO and Advisory Board from primary navigation, and runs a public lot-linked COA lookup with a named lab. The gaps are in label granularity (cannabinoids grouped as a proprietary CBD + CBDA total), COA panel scope (potency-only on the surfaced certificate), and facility-level manufacturing identity, which stays at region and corporate-HQ level.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreePublic COA LookupPer-Lot TraceabilityNASC MemberFinished-Formula TrialNamed Mfg Facility
What's in it
Publishes roughly 18 studies with author, institution, journal, and direct links, the majority peer-reviewed finished-formula trials on ElleVet's own CBD + CBDA blend rather than borrowed ingredient research.
Surfaces a fully named Chief Medical Officer (Dr. Joseph Wakshlag, DVM, PhD, DACVIM, DACVSMR) and a deep Advisory Board of board-certified diplomates with detailed bios, reachable from primary navigation.
Operates a public, self-serve, lot-linked COA lookup with the third-party lab (ProVerde) named, and publishes detailed receptor-level ingredient mechanism content on its Science page.
What's not in it
Cannabinoid actives are disclosed as a combined CBD + CBDA total under a proprietary complete-spectrum label across the line, with minor cannabinoids and terpenes unquantified per serving.
The publicly pullable COA shows cannabinoid potency only; the heavy-metal, pesticide, and microbial panels described in the FAQ are not surfaced on the lot certificate.
No dedicated manufacturing, quality, or sourcing page exists; the manufacturing/extraction facility is not named at facility/city/state level and no cGMP, FDA-registered, HACCP, SQF, or ISO certification is disclosed beyond the NASC seal.
Why this score
itap any criterion for evidence
——
Why this score
What's missing
Brand's own words
Every reviewed PDP publishes a per-serving active panel with defined serving sizes and a full alphabetical inactive-ingredient list. The Soft Chews disclose Glucosamine (Shellfish) 340mg / 510mg and Chondroitin (Bovine) 140mg / 210mg per small and large chew respectively, and all cannabinoid SKUs state a combined CBD + CBDA milligram figure: oil at 70mg/mL, soft gels at 3.8mg / 11.3mg / 28mg / 37.5mg per size, and Calm & Comfort at 46mg per 6g chew. The limiting pattern is line-wide rather than SKU-specific: the cannabinoid actives are presented as a proprietary complete-spectrum total ('ElleVet Complete Spectrum Proprietary Hemp Oil 20mg (contains 12.8mg of CBD + CBDA and other minor cannabinoids)') rather than itemizing CBD and CBDA separately, and the minor cannabinoids and terpenes are never quantified per serving on the label. The example COA for lot R9005-14 does break the blend into CBD 34.565 and CBDA 33.033 mg/mL, so the split is verifiable at the batch level even though it is grouped on the panel. Disclosure is therefore strong and consistent on the primary actives but relies on a grouped, proprietary-blend figure for the cannabinoid component across the whole line.
The score is held below 8 because the cannabinoid actives are disclosed as a combined CBD + CBDA total under a proprietary complete-spectrum label across every SKU, and the minor cannabinoids and terpenes are unquantified per serving. Itemizing CBD and CBDA separately on the panel and publishing per-serving amounts for the minor cannabinoids and terpenes (rather than 'and other minor cannabinoids') would lift it toward 9-10.
Soft Chews contain our proprietary oil formulation, as well as glucosamine and chondroitin.
The /cbd-science/ page is an unusually deep ingredient-rationale resource for the category. It explains the endocannabinoid system and then names the specific receptor systems ElleVet attributes the response to, walking through TRP channels, GPR55, PPAR-g, the 5HT1A and 5HT3A serotonin receptors, the glycine receptor, and adenosine transport, and explicitly argues the CB1/CB2 receptors are not the operative mechanism at achievable serum concentrations. It separates the biological roles of CBDA versus CBD (CBDA absorption and serotonin/anti-inflammatory effect), describes FAAH enzyme inhibition, and gives terpene-by-terpene rationale (myrcene, limonene, alpha-pinene, beta-caryophyllene, humulene, linalool) plus the entourage effect. The glucosamine and chondroitin in the chews appear as named label actives without a comparable mechanism or benefit explanation on the reviewed pages. Because the cannabinoid blend is the core active across the entire line and its mechanism is documented exhaustively with supporting research cited on the same page, rationale coverage is near-complete.
The score sits at 9 rather than 10 because the secondary joint actives (glucosamine, chondroitin) are surfaced as label ingredients without a mechanism explanation, and mechanism content is concentrated on the central Science page rather than restated per product. Adding ingredient-level mechanism and citations for glucosamine and chondroitin would complete the criterion.
ElleVet’s research has shown that it is far more complex and that the receptors involved include the TRP, GPR, PPAR-g GPR55, 5HT, glycine, and adenosine uptake receptors.
ElleVet's research disclosure is the strongest element of its surface. The Science page lists roughly 18 studies, each with a title, date, study design, quantified result, named lead researcher (Wakshlag, Deabold, Court), institution (Cornell, University of Florida, Washington State, Utrecht), journal or publisher, and a direct link to the publication in Frontiers, MDPI, Wiley, Dovepress, SAGE, or AVMA journals. Crucially, the trials are run on ElleVet's own finished CBD + CBDA blend rather than borrowed ingredient research: the oil is described as 'the exact blend that is used in our clinical trials', and there are published finished-formula studies on mobility (Cornell), sensitive skin (a randomized, double-blinded, placebo-controlled trial, n = 17 treated), neurological events, feline mobility, and safety/drug-interaction work. The For Veterinarians page states the brand has 'completed and published more than 20 peer-reviewed studies' as of January 2026. The brand distinguishes its finished-product evidence clearly and does not present unrelated ingredient trials as finished-formula proof.
The criterion's 10 anchor is met. The only residual nuance is that several of the more recent reports (Calm & Comfort, dental stick, equine pellets, feline urinary) are white papers hosted on the ElleVet domain rather than peer-reviewed journal articles; labeling each report's peer-review status inline would remove any ambiguity between published trials and self-hosted white papers.
Dogs were randomly assigned to receive either 2 mg/kg of an equal mix of CBD/CBDA rich hemp from ElleVet Sciences (n = 17) or placebo for four weeks.
Named expert disclosure is comprehensive and reachable from primary navigation (About > Meet the Team). Dr. Joseph Wakshlag is surfaced as Chief Medical Officer and Chair of the Advisory Board with full credentials (DVM, PhD, DACVIM Nutrition, DACVSMR, Professor at Cornell) and a documented role and scope: he conducted the first ElleVet clinical trial and the first pharmacokinetic and safety studies. Beyond him, a full Advisory Board of board-certified diplomates is listed with detailed bios, including specialists across surgery and sports medicine (Adair, Kaneps), behavior (Albright), dermatology (Santoro, whose specialty maps to the published skin trial), internal medicine and cardiology (Ettinger, Kornreich), orthopedics and osteoarthritis (Kirkby Shaw), neurology (Wininger), pharmacovigilance (Elam, also ElleVet's Director of Pharmacovigilance), and regulatory science (McChesney, a former FDA CVM compliance director). Two staff veterinarians, Dr. Robert Menardi (Senior Director of Veterinary Education) and Dr. David Tittle (International Scientific Advisory Board), have dedicated bio pages with credentials and scope.
The 10 anchor is met. A minor refinement would be to name a single lead formulator for the finished products; the formulation is attributed to the founders working with biochemists and to Dr. Wakshlag's research rather than to one named formulator, though the CMO and advisory disclosure more than satisfy the criterion.
Dr. Wakshlag conducted the first ever clinical trial on dogs using ElleVet CBD + CBDA and continues to lead the way in hemp research.
ElleVet operates a genuine public, self-serve, lot-linked COA program. The COA library explains where the batch number is printed on each SKU and provides a search field ('enter batch number here') that returns the matching certificate, and a live example for lot R9005-14 confirms lot-level traceability with a full cannabinoid potency panel (CBD 34.565, CBDA 33.033, D9-THC 1.837 mg/mL, total cannabinoids 75.367). The third-party laboratory is named: ProVerde. The FAQ additionally describes a multi-stage third-party testing program in which the extract is tested for contaminants and final batches are tested for potency. The limiter is panel scope on the surfaced certificate: the COA a buyer can actually pull is potency/cannabinoid-only and does not display the heavy-metal, pesticide, microbial, or residual-solvent results that the FAQ says are tested upstream.
The score is held at 9 because the publicly accessible COA surfaces cannabinoid potency only; the contaminant and microbial panels are described in FAQ prose but their results are not shown on the lot certificate. Publishing the heavy-metal, pesticide, microbial, and residual-solvent results on each lot's COA would complete the 10 anchor.
Proverde, the 3rd party lab that tests our products, does not test for CBCa, which accounts for 2-3% of our profile.
ElleVet discloses a recognized quality-system seal and a clear sourcing narrative, but holds facility identity above the facility level. The FAQ states NASC membership ('We are proud to display the NASC Quality Seal', with the NASC seal image also rendering on the home page) and provides sourcing logic: the brand says it controls 'our products entire cycle - from the farm to the end-user', that it does 'not buy from a bulk manufacturer', that the hemp is a proprietary cultivar grown under 'strictly controlled growing in Colorado', and (on the Hemp page) describes cold hydrocarbon extraction as its preferred method. What is not disclosed is the manufacturing or extraction facility at name/city/state level: probes of /manufacturing/, /quality/, /sourcing/, /gmp/, and /certifications/ all return 404, and the only street address published is the corporate HQ at 200 John Roberts Rd., South Portland, Maine. No cGMP, FDA-registered-facility, HACCP, SQF, or ISO certification is named.
The score is held at 8 because the quality system surfaced is NASC plus sourcing logic, while facility identity stays at region (Colorado growing) and corporate-HQ level rather than naming the manufacturing/extraction facility. Naming the facility (name, city, state) and disclosing a facility certification such as cGMP or FDA registration would lift it toward 9-10.
At ElleVet, we control our products’ entire cycle - from the farm to the end-user. We do not buy from a bulk manufacturer.
ElleVet's claims are unusually well supported relative to the category, yet the framing runs confident. The home hero carries an unqualified 'Scientifically Proven' badge and product pages use 'proven' language ('Our proprietary CBD + CBDA has been proven to help decrease joint discomfort'), while the broader marketing leans on superlatives such as being 'the only product proven effective in multiple clinical trials.' These claims do trace to real published finished-formula trials, the site consistently carries the FDA structure/function disclaimer ('not intended to diagnose, treat, cure or prevent any disease'), review modules state results 'are not guaranteed, are not medically substantiated', and the home page qualifies its vet-endorsement claim with a footnote naming the Cornell double-blind study. The brand avoids overt disease-cure language. The remaining tension is that the strong 'proven' framing appears above the fold with the supporting citation living a click away on the Science page rather than inline; the per-benefit support claims are more cautiously worded (the home page frames the neurological benefit as 'CBD + CBDA can support healthy brain function'), so the headline 'Scientifically Proven' badge and the comparative 'only product proven' superlatives carry the confident framing without an inline citation.
The score is held at 8 because confident 'proven'/'Scientifically Proven' framing appears above the fold without an inline citation or qualifier, and the comparative 'only product proven' superlatives sit a click away from their supporting studies rather than beside the claim. Moving the specific study citation inline beside each 'proven' claim and superlative would lift it toward 9-10.
Our proprietary CBD + CBDA has been proven to help decrease joint discomfort and improve overall mobility, allowing your dog to get back to doing what they love.
Three of the four evidence pillars are reachable with little effort. The Science (mechanism and study list) lives on a top-level 'Science' nav item, and named experts are one level down under About > Meet the Team, both in the primary header. Testing is reachable through the footer 'Certificate of Analysis' link, which opens a working self-serve batch lookup. The weaker pillar is manufacturing and sourcing: there is no dedicated manufacturing, quality, or sourcing page (those URLs 404), so a buyer must dig into the FAQ to find the Colorado-growing and farm-to-end-user disclosures. Evidence is also split between header and footer rather than gathered into a single consolidated trust hub, and the research list and COA library are footer-only.
The score is held at 8 because the COA library and research list are footer-only, manufacturing/sourcing detail is buried inside the FAQ with no dedicated page, and there is no single consolidated 'Evidence & Trust' hub. Promoting testing and sourcing into primary navigation or a consolidated trust hub would lift it toward 9-10.
First, you will need to find the batch number specific to your product.
ElleVet Sciences sits well above the category median on research and expert disclosure: it cites peer-reviewed finished-formula trials with authors and journals, names a credent...
Fera Pets presents above the DTC median on named-expert disclosure and operates a real lot-linked COA lookup. The brand publishes mechanism content with ingredient-level citations and avoids disease-treatment claim language. Substance gaps cluster on the legacy product line — flagship chewables disclose every active dose while powders and toppers fall back to total-blend amounts — and on facility-level manufacturing identity, which is held at country and certification-body level only.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreePublic COA LookupPer-Lot TraceabilityNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
Fully named five-member Vet Advisory Board with two ACVIM/ACVD board-certified diplomates and disclosed credentials — one of the stronger named-expert disclosures in the DTC pet supplement universe.
Functional lot-linked COA lookup tool accepting LOT numbers or product names — real buyer-usable testing transparency rather than a placeholder badge.
Brand-level Ingredients encyclopedia publishes per-ingredient mechanism content with linked peer-reviewed studies for most meaningful actives, including ashwagandha, milk thistle, glucosamine, and probiotic strains.
What's not in it
Label transparency varies materially across the line: chewable SKUs disclose every active in mg / IU / CFU while legacy powders (Probiotic Supplement, Mushroom Blend, Whole Food Multivitamin Topper) use total-blend amounts or generic descriptors.
Manufacturing facility is not named at facility / city / state level — only 'manufactured in the USA in an FDA-registered GMP facility, NASC certified' country-level disclosure.
COA panel scope (which contaminants, microbials, potency assays) is not surfaced on the public Sustainability hub; third-party lab (Eurofins) is named only on the Fish Oil PDP rather than consistently across the line.
Why this score
itap any criterion for evidence
——
Why this score
What's missing
Brand's own words
Disclosure tier varies materially across the line. The chewable and liquid SKUs reviewed (Hip + Joint Support, Multivitamin Soft Chews, Wellness Blend for Cats, Fish Oil for Dogs) publish full per-active mg/IU/CFU panels with inactives, serving sizes, and (in Wellness Blend and Multivitamin Chews) strain-level probiotic identifiers. The legacy powder SKUs are weaker: USDA Organic Probiotic Supplement names 12 species at genus/species level only with a total CFU rather than per-strain CFU; USDA Organic Mushroom Blend discloses a 500 mg total blend across ten mushroom species without per-species mg amounts; Whole Food Multivitamin Topper lists key ingredients with mechanism descriptors but no per-active doses. Brand uses 'proprietary blend' marketing language on Hip + Joint despite the active panel being fully numerically disclosed — verbal friction without actual obfuscation. Modal-product score reflects the dispersion: the flagship chewables clear an 8, but powders and toppers do not.
Legacy powder SKUs (Probiotic Supplement, Mushroom Blend, Whole Food Multivitamin Topper) do not publish per-active amounts at the disclosure tier the chewable SKUs achieve. Strain-level CFU is named on Wellness Blend and Multivitamin Chews but not on the flagship Probiotic Supplement.
Our Mushroom Blend has anywhere between >16-50% Beta Glucans. It changes between batches due to variations in mushrooms.
The brand-level Ingredients encyclopedia publishes per-ingredient mechanism content — biological role, plausible action, and selection rationale — for the majority of meaningful actives in the line. PDPs reinforce mechanism framing at the product level (turmeric, glucosamine, MSM, postbiotic action, lysine/taurine roles). The Ingredients page filters by both product and benefit category, which is a buyer-usable structure rather than a marketing-copy dump. Where it falls short of a 9 is uniformity: legacy SKUs (Mushroom Blend) describe ingredients in benefit terms more than mechanism terms, and the Whole Food Multivitamin Topper's mechanism content is single-sentence per ingredient. The brand does not publish a unifying scientific framework or finished-formula design rationale separate from per-ingredient logic.
No brand-level scientific framework explaining finished-formula design (versus per-ingredient mechanism). Mechanism content is uneven across the line — strong on flagship chewables, thinner on legacy powders.
Silymarin is a powerful antioxidant that supports normal inflammatory response.
Citation discipline is present and uneven. Hip + Joint cites four studies including a peer-reviewed glucosamine/chondroitin review; Multivitamin Soft Chews link a randomized double-blind glucosamine/chondroitin trial AND a Bacillus subtilis DE-CA9 study; Wellness Blend for Cats links three peer-reviewed papers (green-lipped mussel, cranberry, taurine); the Ingredients hub links additional studies (ashwagandha, milk thistle, etc.). All cited research is ingredient-level rather than finished-formula. The brand uses 'clinically studied probiotic' for the named strain (DE-CA9) — which is defensible because the strain itself has a published trial — but does not separately publish a finished-formula clinical study. The brand also avoids 'clinically proven' language at the product level, which is the right call given the actual evidence inventory. The flagship USDA Organic Probiotic Supplement is the weak point: 12 species listed without strain identifiers means the linked prebiotic studies do not function as evidence for the probiotic claim.
No finished-formula clinical trial published or referenced. Citation depth varies — flagship chewables carry multiple studies; the legacy probiotic SKU carries only prebiotic-component studies without strain-level probiotic evidence.
Bacillus subtilis DE-CA9 effect on fecal scores and serum oxidative markers in healthy dogs.
Five named veterinarians are surfaced with credentials, photographs, and biographical detail on a dedicated Vet Advisory Board page reachable from the footer and the mega-menu. Two of the five hold ACVIM or ACVD board specialty diplomate status — a substantive tier above the generic 'our vet team' framing that defines most DTC competitors. The founder Dr. Michelle Dulake (DVM, acupuncturist) is named and credentialed as formulator; her education, internship, and certifications are all disclosed. Where the disclosure falls short of a 10 is scope-of-involvement specificity: the brand describes the board as 'advisory' without explicitly disclosing per-product review responsibility, formulation veto power, or named ownership of specific SKUs. Buyers can verify WHO the experts are; they cannot fully verify WHAT each expert did on which product. Still, this is one of the stronger named-expert disclosures in the DTC pet supplement universe.
Scope of involvement is described in general advisory terms without explicit per-product review attribution or formulation authorship beyond the founder.
Fera operates a real, functional, lot-linked COA lookup tool accessible from the Sustainability page. The tool accepts LOT numbers or product names, and Eurofins is named on the Fish Oil product page. Those facts meet rubric tier 8: third-party testing is publicly described, at least one laboratory is named, and buyer access is stronger than an on-request-only program. It does not reach tier 9 because laboratory identity is not consistent across the line, the Sustainability hub does not summarize contaminant, microbial, potency, pesticide, or identity panels by SKU, and public records do not establish complete lot-lookup coverage for every product.
Test-panel scope is not summarized by SKU on the public Sustainability hub. Lab identity (Eurofins) is named only on the Fish Oil product page, and complete lot-lookup coverage is not established consistently across the line.
Every Fera Pets batch is tested by certified 3rd party labs.
Fera says its supplements are manufactured in the USA with domestic and imported ingredients at an FDA-registered GMP facility, and it publishes NASC Seal of Quality language. That is a disclosed quality system with country-level manufacturing identity and matches rubric tier 8. It does not reach tier 9 because Fera does not name the facility, city, or state; sourcing logic is only partial (for example, fish-oil geography); and the public NASC material does not disclose Fera's audit date, scope, or findings.
Manufacturing identity stops at the country level; facility name, city, and state are not public. Sourcing logic is sporadic, and Fera-specific NASC audit findings and dates are not disclosed.
All our supplements are manufactured in the USA with domestic and imported ingredients in an FDA-registered GMP facility, and NASC certified.
Brand marketing stays inside supportable claim language. Product benefits are framed as 'supports,' 'helps,' 'eases occasional stiffness,' 'maintains healthy cartilage' — not disease-treatment or cure language. The home page hero does not assert 'clinically proven' or 'veterinarian-approved' claims; promotional copy emphasizes discounts and category positioning rather than clinical certainty. Where the brand uses 'clinically studied,' it points specifically to the named strain (DE-CA9) that does have a published trial — defensible. Fera does NOT publish disease-state claim language on the surveyed surface. The score holds below 9 because (a) the home page does not carry above-the-fold qualifying language ('not intended to diagnose...') visible to a casual buyer, (b) some product copy uses 'proprietary blend' marketing language even when the active panel is fully numerically disclosed, and (c) the brand's 'Vet Created' phrasing is broader than the actual scope of the Vet Advisory Board's per-product role.
No above-the-fold safety qualifier. 'Vet Created' framing implies a tighter formulation tie than the advisory board's disclosed scope. 'Proprietary blend' marketing on dose-disclosed panels creates avoidable verbal friction.
Helps Relieve Occasional Joint Stiffness
Evidence pages are reachable within three clicks from the home page. Header navigation surfaces About and a quiz; the mega-menu and footer carry direct links to About Us, Vet Advisory Board, Sustainability (which hosts the COA lookup tool), FAQ, Ingredients, Store Locator, and Blog. The four pillars all have findable surfaces: science (Ingredients), evidence (PDP citations), experts (Vet Advisory Board), testing (Sustainability + COA Lookup). The accessibility ceiling is set by the absence of a single consolidated 'trust hub' — pillars are distributed across separate pages, so buyers must navigate to multiple destinations rather than landing in one evidence index. The home page above-the-fold also leads with promotional copy, not evidence framing.
No single consolidated trust / evidence hub. Above-the-fold home page emphasizes promotions rather than evidence routing. Pillars are reachable but distributed.
Utilize our COA search tool to check your product's test results.
Fera Pets presents above the DTC median on named-expert disclosure and operates a real lot-linked COA lookup. The brand publishes mechanism content with ingredient-level citatio...
AnimalBiome is the strongest evidence system in this batch on science, named experts, and donor/batch screening, with verifiable citations to NEJM and PubMed Central for its FMT-effectiveness claims. It is weaker on manufacturing and COA disclosure, which were not found anywhere on the public site despite an exhaustive search, and on finished-product claim discipline: one product page makes an unqualified 'scientifically proven' disease-symptom claim with no citation, and the pilot study's own linked publication is sponsored trade content rather than peer-reviewed research.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
Named scientific and veterinary leaders, including four named PhDs, are publicly visible on the team page under primary navigation.
Gut Restore donor and batch screening names two independent third-party labs (IDEXX Reference Laboratories and Antech Diagnostics) with specific pathogen panels.
The Gut Restore product page links its FMT-effectiveness claims to real, independently verifiable NEJM and PubMed Central sources, not just its own pilot data.
What's not in it
No public lot-linked COA lookup, finished-product batch report, or manufacturing facility/certification disclosure was found anywhere on the site after an exhaustive search.
The pilot study's linked '2019 publication' is sponsored trade-press content, not a peer-reviewed journal article, and mixes AnimalBiome's own uncontrolled pilot data with borrowed third-party FMT research.
Conventional dose/potency metrics are not disclosed for the flagship Gut Restore capsule, and a secondary product (Skin Rescue) groups eight ingredients into one undisclosed-by-species proprietary blend.
Why this score
itap any criterion for evidence
——
Why this score
What's missing
Brand's own words
Disclosure is uneven across the line, which is what keeps this below the top tiers even though two of three checked non-flagship products disclose fully. On the flagship Gut Restore, AnimalBiome discloses the active source material, inactive ingredients, Small/Medium/Large capsule-size variants, and weight-based use directions, but the Active Ingredients panel names only the source material (screened fecal matter) with no CFU, strain/species composition, or batch-specific microbial-abundance figure -- a structural gap inherent to an FMT/donor-material product rather than a proprietary-blend concealment. Verification pulled two additional product pages to test the modal line: S. boulardii + FOS discloses full per-active quantities ('Saccharomyces boulardii CNCM I-3799, 6.6 Billion CFU' and 'GOFOS(TM), 225 mg' per scoop) with Inactive Ingredients stated as 'None' and no blend. Skin Rescue discloses most actives by per-weight-tier mg amount but groups eight mushroom species into a single 'Organic Mushroom Blend' mg total without species-level breakout, which is a genuine grouped/proprietary-style disclosure gap on a secondary product. That mix -- one fully quantitative product, one mostly quantitative product with one grouped blend, and a flagship with no quantitative active panel at all -- matches tier anchor 7 ('Disclosure is strong on the flagship but inconsistent across the broader line -- multiple products use proprietary blends or grouped amounts') more closely than anchor
The flagship's active identity and use directions are public, but microbe counts, community composition, and lot-specific potency-style metrics are not disclosed in a standard panel; a secondary product (Skin Rescue) also groups eight ingredients into one undisclosed-by-species mushroom blend.
Extensively-screened canine fecal material sourced from healthy donors who are fed a balanced diet.
AnimalBiome publishes a clear scientific rationale for microbiome testing and FMT-style supplementation, and verification confirmed this extends past the flagship. The science page explains sequencing, healthy reference sets, missing beneficial bacteria, harmful bacteria, and restoration logic mapped to product categories. The Gut Restore PDP and donor-screening page connect the formulation to screened donor material and delayed-release capsules. Verification pulled two secondary products to test consistency: the S. boulardii + FOS page carries dedicated 'About Saccharomyces boulardii' and 'About Fructooligosaccharides (FOS)' sections that explain mechanism specifically -- e.g., that S. boulardii is a yeast (not bacteria) that survives stomach acid and produces short-chain fatty acids that support the gut barrier, and that FOS is a prebiotic fiber that feeds beneficial microbes -- which is genuine ingredient-level mechanism content, not just benefit language. Skin Rescue's rationale is thinner by comparison (a 'gut-skin axis' and 'postbiotic' framing with per-ingredient callouts, e.g. quercetin as 'nature's benadryl') but still connects ingredients to a stated mechanism rather than benefit assertions alone. This pattern -- flagship and most secondary products carrying real rationale, with only one secondary product's mechanism explanation being noticeably thinner -- matches tier anchor 9 ('rationale is published for the flagship and most secondary products, with only minor me
The microbiome mechanism is well explained on the flagship and on S. boulardii + FOS, but Skin Rescue's ingredient-level rationale is comparatively thinner, and several 'studies have shown' mechanism claims on secondary products are not linked to a specific citation on-page.
We are a company founded and led by scientists, taking an innovative and scientific approach to everything we do.
AnimalBiome goes beyond generic research-backed language by publishing a pilot-study page with real first-party finished-formula data: sample sizes (40 dogs, 72 cats), intervention duration (25 days), and improvement percentages measured on the actual Gut Restore capsule, not just an ingredient. That first-party data is a genuine strength. Verification independently fetched the '2019 publication' the pilot page links out to and read it in full: it is a 'SmartFocus on Animal Health' trade-press update explicitly marked 'SPONSORED BY' AnimalBiome, not a peer-reviewed journal article -- it has no visible journal name, DOI, or peer-review indicator, and it presents AnimalBiome's own uncontrolled pilot percentages in the same document as a numbered-reference literature review citing several independent third-party FMT studies in dogs and cats, without a clear on-page line between 'this is category-level FMT research by other investigators' and 'this is our own product's pilot data.' Verification also checked citation discipline on a secondary product page, S. boulardii + FOS, and found a mixed pattern: the claim that S. boulardii is 'safe and effective for cats and dogs' is inline-hyperlinked to a real British Veterinary Association / Wiley journal article, but two adjacent 'studies have shown' claims on the same page (about antibiotic-associated diarrhea and about FOS improving gut/immune function) carry no citation or link at all. Together, a real first-party pilot, a sponsored
The pilot study is public and first-party, but the page does not expose a controlled-trial design or journal metadata, its linked 2019 write-up is sponsored trade content rather than a peer-reviewed publication, and on a secondary product page (S. boulardii + FOS) two of three 'studies have shown' claims are not linked to a citation even though one adjacent claim is.
Each pet was given an AnimalBiome Gut Restore Supplement (fecal transplant in a capsule) twice per day, for 25 days.
AnimalBiome publicly names scientific and veterinary leaders, including a PhD co-founder/chief science officer and a DVM/MSc/PhD VP of Microbial Discovery. Verification confirmed the Meet the Team page is reachable through the primary navigation (nested under the 'About Us' menu, not footer-only or search-only) and, on refutation-probing that same already-cited page, found two additional named PhDs beyond the two originally logged: Connie Rojas, PhD (Director of Field Trials and Senior Scientist) and Katie Dahlhausen, PhD (Product Manager II, Supplements) -- the latter role title explicitly ties a named PhD to the Supplements line. The Our Company page independently corroborates Holly Ganz's Founder/Chief Science Officer role. That combination -- at least one named expert (in fact several) fully surfaced with credentials and role, secondary expert involvement documented across additional named PhDs, reachable via primary navigation -- matches tier anchor 9 rather than anchor 8, which is reserved for names reachable only via deep navigation or with partial credentials. It falls short of anchor 10 because no biographical context or explicit scope-of-involvement narrative is given for any named person -- titles are stated but not what each person actually does day-to-day, and no page states which named person reviewed or signed off on a specific formula.
Named credentials and titles are visible for multiple scientists, but no page states biographical context or which named person reviewed or signed off on a specific formula.
Niokhor Dione, DVM, MSc, PhD
AnimalBiome discloses a substantive screening program for Gut Restore donor material. Verification read the donor-screening page in full and found it names two independent third-party laboratories, not one -- IDEXX Reference Laboratories and Antech Diagnostics -- and states the pathogen/parasite PCR panel covers 'routine donor and batch screening,' listing specific named organisms (e.g. Salmonella spp., Giardia spp., canine parvovirus 2, Toxoplasma gondii) rather than generic 'we test for pathogens' language. This is unusually specific for a microbiome supplement. Verification also actively searched for a COA or lab-report page: the full sitemap (159 /pages/ URLs) was enumerated and no COA, lab-results, certificate-of-analysis, or batch-report page was found, and none of the 12 pages fetched during this review contain COA text. That absence held up under refutation attempts. Because lot-level COA access here is not 'partial or available on request' (tier anchor 8) but is not present in any form, and the disclosed testing -- while lab-named and detailed -- is not connected to a buyer-visible specific lot or finished-capsule potency figure, this stays at tier anchor 7 ('Testing is referenced publicly, but COA access is limited, generic, or not connected to specific lots') rather than moving up to anchor 8.
Donor and batch screening is detailed and names two labs (IDEXX, Antech), but no public lot-linked COA, finished-capsule potency report, or on-request COA statement was found anywhere on the site after a full sitemap search.
Donor stool samples are submitted for parasites and pathogen screening to the IDEXX Reference Laboratories
AnimalBiome discloses quality-control intent and substantial donor-material sourcing logic, but not a facility-level manufacturing system. The science page states quality and safety are central and references third-party testing and 'gold standard' quality-control processes, but that sentence names no facility, certification body, or lab. The donor-screening page gives strong, verified input-control detail (two named labs, specific pathogen panels). Verification actively searched for manufacturing/facility disclosure across all 12 archived sources plus the full 159-URL /pages/ sitemap and the Our Company (about/mission) page: no cGMP, HACCP, FDA-registration, NASC membership, SQF, or ISO certification term appears anywhere, and no facility name, city, or state for capsule production is disclosed (the only address found is the Oakland, CA corporate/HQ address on the patents and contact pages, not a stated manufacturing site). This mixed picture -- real, specific, verifiable sourcing/screening detail for donor input material, but zero verifiable disclosure for the actual manufacturing/production step -- keeps this at the middle tier rather than the more generic anchor 4 (which requires no sourcing detail at all, not met here) or a higher anchor (which requires named facility or certification, not found after an exhaustive search).
The public pages do not name a manufacturing facility, disclose cGMP/HACCP/FDA-registration/NASC/SQF/ISO status, or state batch-release rules for finished capsules, despite a full-site search including the sitemap and about-us page.
We conduct third party testing on our supplements and follow the gold standard of quality control processes.
AnimalBiome's claim discipline is genuinely mixed rather than uniformly weak, which verification confirmed in both directions. On the Gut Restore PDP, the above-the-fold headline 'Resolve the root cause of diarrhea, soft stools, and itchy skin' is an assertive claim, but elsewhere on that same page the statement that FMT 'has proven to be an effective treatment' is inline-hyperlinked to a real New England Journal of Medicine article (nejm.org) for the human-medicine claim and a PubMed Central article (ncbi.nlm.nih.gov/pmc) for the companion-animal claim -- real, checkable citation discipline for a modality-level claim. Against that, verification found an uncited claim on a different product: the Skin Rescue page states its postbiotic ingredient is 'scientifically proven to reduce symptoms of atopic dermatitis in cats and dogs' with no inline citation, link, or footnote anywhere on that page. That combination -- disciplined, verifiably-cited claims on one product page and an unqualified 'scientifically proven' disease-symptom claim with zero citation on another -- matches tier anchor 7 ('Mixed -- some product pages or marketing campaigns make claims that the brand's evidence cannot fully support') rather than the lower anchors, which require citation discipline to be essentially absent or unverifiable brand-wide.
The Gut Restore PDP's FMT-effectiveness claims are cited to NEJM and PubMed Central, but the same page's above-the-fold 'Resolve the root cause' headline and the Skin Rescue page's uncited 'scientifically proven' atopic-dermatitis claim are not qualified or linked to a specific study.
Resolve the root cause of diarrhea, soft stools, and itchy skin
Verification confirmed three of the four evidence pillars are reachable directly from the home page's primary navigation: Our Science and Gut Restore (FMT) Donor Screening sit under the 'Learn More' mega-menu, and Meet the Team sits under 'About Us' -- all one to two clicks away, none footer-only. The Pilot Study page (a fourth science-adjacent evidence page) is not linked from primary navigation at all (zero direct home-page links found) and is reachable only via a blog-style 'Learn More About IBD' link or a direct URL. The fourth rubric pillar, manufacturing, could not be found anywhere on the public site after an exhaustive search across all 12 archived sources and the full 159-URL /pages/ sitemap -- that is a harder accessibility failure than deep navigation, since no click depth surfaces content that was not found to exist. Site scale was independently verified: three sitemap segments alone (pages, products, blog) total 283 URLs, corroborating a 'hundreds of URLs' characterization. No consolidated single trust hub (e.g. an 'Evidence & Trust' page) was found; every 'transparency' hit on the home page resolved to review-widget configuration JSON, not a navigation item. This combination -- most evidence reachable via primary nav and distributed rather than hubbed, but one full pillar (manufacturing) not found anywhere and one science-adjacent page (Pilot Study) requiring off-nav discovery -- keeps this at tier anchor 8 rather than moving to anchor 9, which presumes all evid
Science, testing, and named experts are reachable from primary navigation, but manufacturing evidence was not found anywhere on the site after an exhaustive search, and the Pilot Study page requires off-navigation discovery.
AnimalBiome is the strongest evidence system in this batch on science, named experts, and donor/batch screening, with verifiable citations to NEJM and PubMed Central for its FMT...
PetLab Co presents well above the DTC median on named-expert disclosure and claim qualification: a seven-member named advisory board with per-member scope of involvement, formulation-scope credits, and footnoted clinical claims with study durations and endpoints. Label panels are structured line-wide, with proprietary-blend totals on probiotic SKUs. Its Probiotic Chew finished-formula study is published in a peer-reviewed journal and identifiable by named author, but the brand does not link it on-site, the ProBright Advanced studies are not published or identified, no laboratory is named, and no COA or lot lookup exists — so most testing and clinical claims still cannot be inspected before purchase.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
Named-expert disclosure is among the deepest in the DTC set: a seven-member Scientific Advisory Board in primary navigation, each member carrying a credentialed bio plus an 'At PetLabCo.®' statement of their specific role, formulation-scope credits for Dr. Greg Sunvold, Ph.D. and Dr. Jan Bellows (American Veterinary Dental College), and a named reviewing veterinarian (Dr. Sarah Cortright, DVM) behind the sitewide 'Vet Reviewed' badge.
Claim qualification is systematic: clinical-style statements carry inline daggers resolving to on-page footnotes with study durations, endpoints, and control-group context; marketing statistics are explicitly labeled as internal subscriber surveys with dates and sample sizes; and the Probiotic Chew finished-formula study is published in a peer-reviewed journal (Zilinger et al., 2026, Pets) and credited on-site by named author.
Label panels are complete and structured on every product reviewed — named actives with per-serving amounts, serving sizes, inactive ingredients, and cautions — reaching per-active mg disclosure with EPA/DHA splits and supplier trademark attribution on the non-probiotic chews.
What's not in it
Of the three cited finished-formula clinical studies, only the Probiotic Chew study is published (peer-reviewed, identifiable by named author); the 28-day and 90-day ProBright Advanced studies are not published or identified by author, journal, or registry, and the brand does not link the published study on its own pages.
Testing claims stop above the artifact layer: no third-party laboratory is named, no certificate of analysis is published, and no lot-level lookup exists anywhere on the brand surface, with common testing/COA URL patterns returning 404.
Probiotic SKUs — including the flagship Probiotic Chews — label actives as proprietary blends with total CFU only, and manufacturing identity is held at 'Manufactured in the USA' country level with no facility name, city, or state.
Why this score
itap any criterion for evidence
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Why this score
What's missing
Brand's own words
Every PDP reviewed publishes a structured Product Facts panel with named actives, per-serving amounts, serving size, inactive ingredients, and cautions — including multi-size SKUs that tabulate doses per chew or scoop size. Joint Care Chews disclose every active in mg per 4 g chew (Glucosamine 450 mg, Green Lipped Mussel 150 mg, Total Omega-3 48 mg with EPA 24 mg / DHA 15 mg splits, Calcium Fructoborate 35 mg, Turmeric 25 mg); Itch Relief Chew Pro and the Multivitamin reach the same tier, down to supplier trademark attributions for AstaReal L10 and Enzalox and a full guaranteed-analysis vitamin panel. The probiotic side of the line holds back: Probiotic Chews label 'A Proprietary Blend of Probiotics (Bacillus coagulans, B. clausii, B. subtilis)' at a total 3 Billion CFU with no per-species counts, and the same blend-total pattern covers Allergy & Immune Chews (1–3 Billion CFU across three sizes), Probiotics for Cats (six species, 2.1 Billion CFU), Anal Gland Support (750 Million CFU), and ProBright Advanced's patent-pending two-species blend. Mobility Pro Oil is the thinnest panel: 'A Proprietary Blend of Curcumin & Zinc Chloride 425 mcg' with no split between the two actives. Modal disclosure is per-active amounts inside a consistent panel template, with a recurring blend-total exception wherever probiotics or blended oils appear — including on the brand's self-described best-selling probiotic flagship.
Proprietary-blend labeling on the probiotic SKUs — including the flagship Probiotic Chews — and the grouped curcumin/zinc figure on Mobility Pro Oil keep the line below the 8 tier. Publishing per-species CFU counts (or strain identifiers with per-strain amounts) and splitting the Mobility Pro Oil blend would lift the score.
A Proprietary Blend of Probiotics (Bacillus coagulans, B. clausii, B. subtilis)
Ingredient rationale is template-consistent across the line rather than flagship-only. Every PDP reviewed carries a 'Research-Backed Active Ingredients' module with a card per active stating its class and physiological role — Glucosamine HCl as 'This amino sugar helps maintain joint lubrication and supports healthy cartilage,' FOS as 'a versatile prebiotic fiber that feeds beneficial bacteria' — and a brand-level Ingredients glossary ('50+ Premium Pet Supplement Ingredients,' reachable from the About menu) repeats per-ingredient purpose blurbs filterable by health area. The About page adds selection logic for hero inputs: non-heat-treated whole Green-Lipped Mussel chosen for 'the highest levels of lipids and omega-3 fatty acids,' and colostrum selected for immunoglobulin and lactoferrin content. Depth, however, stays at one-to-two-sentence role language: meaningful actives are described in benefit-and-role terms rather than worked mechanism explanations, and no ingredient card or glossary entry links to the 'robust scientific research' the brand says stands behind its key ingredients.
Rationale never connects to citable research — no PubMed, journal, or author references appear on any PDP or on the Ingredients glossary. Per-ingredient citations and fuller mechanism write-ups for the major actives would move the score toward 9–10.
every ingredient is carefully selected with a purpose - to target common health issues
PetLab Co's clinical-evidence story is unusually specific for the DTC tier and explicitly scoped to the brand's own finished-formula studies, not borrowed ingredient research. The Ingredients page states 'ProBright® Advanced and Probiotic Chew formulas are backed by clinical studies to demonstrate effectiveness,' limiting finished-formula study claims to two named products, and the claims carry on-page footnotes with design detail: a 28-day hydrogen-sulfide reduction study, 'In a 90-day clinical study, dogs taking ProBright® Advanced daily had a plaque index score that was 25% lower than the control group,' and 'A 29-day clinical study showed using Probiotic Chew daily enhances beneficial gut bacteria.' For the Probiotic Chew, the brand goes further than a footnote: a learn-section article (in the crawl inventory) describes the finished-formula study in full — 'PetLabCo. funded a randomized, placebo-controlled clinical study,' 24 healthy adult Beagles for 31 days, Day 0/14/31 sampling, a reduction in fecal calprotectin, and all three Bacillus species increasing — and attributes it inline to a named first author and year, '(Zilinger et al., 2026).' That study is genuinely published and identifiable: Zilinger et al. (2026), 'Effect of a Supplement Containing Probiotics, Prebiotics, and Yeast Extract on Gut Inflammation, Microbiota, and Cytokines in Healthy Dogs,' Pets (MDPI), DOI 10.3390/pets3010001 — a peer-reviewed, open-access paper whose composition matches the Probiotic Ch
One finished-formula study (Probiotic Chew) is published and identifiable by named author, but the brand does not hyperlink it from the PDP or the learn article, and the ProBright Advanced 28-day and 90-day studies carry no author, journal, registry entry, or link. Directly linking the published Probiotic Chew paper and publishing or identifying the two dental studies (author, venue, or registry) would lift the score toward 8; peer-reviewed publication of all three with on-page citations would support 9–10.
In a 90-day clinical study, dogs taking ProBright® Advanced daily had a plaque index score that was 25% lower than the control group.
The Experts entry in the primary About menu opens 'PetLabCo.®'s Scientific Advisory Board,' naming seven individuals with photos, titles, and capsule credentials: Gregory D. Sunvold, Ph.D. (Chief Scientist), Dr. Jan Bellows (Board Certified Veterinary Dentist, American Veterinary Dental College, practicing since 1977), Dr. Gavin Casper (Fear-Free certified veterinarian), Jessica Bagel (Clinical Trial Manager, DVM graduate from NCSU with 13+ years at UPenn), Dr. Margie Scherk (feline specialist, board-certified since 1995), Dr. Stephanie McGrath (Associate Professor of neurology at Colorado State University), and Dr. Matt Kaeberlein (Co-Director of the Dog Aging Project). Beyond credentials and a full external-career biography, each member's on-page 'Meet Dr. [name]' profile carries an 'At PetLabCo.®' block stating that member's specific scope of involvement: Sunvold 'leads product formulation science' and co-authors clinical trial protocols and reports; Bellows serves as Chief Dental Specialist 'helping with product formulation and testing, clinical trial protocol design and report authoring'; Bagel runs clinical-trial protocol design and execution; Casper reviews ingredients for joint-health effectiveness; Scherk 'helped in the development of our first Cat Product – Cat Probiotic'; McGrath leads protocol design of the senior-dog/Longevity trial with Colorado State University as the executing CRO; and Kaeberlein collaborated on the Longevity supplement and its trial protocol.
Disclosure meets the 10 anchor: seven named advisors reachable from primary navigation, each with credentials, a full biography, and an 'At PetLabCo.®' scope-of-involvement statement. Two minor refinements remain — the per-member PetLab scope sits one click into each card's profile panel rather than in the always-visible capsule, and the formula-reviewing veterinarian named in the home FAQ (Dr. Cortright) is surfaced on the home page but not added to the Experts roster itself.
Every formula is thoroughly reviewed by Dr. Sarah Cortright, DVM, our trusted Veterinary Consultant at PetLabCo.®
Testing disclosure is assertion-level. The About page commits to batch testing in named categories — 'Every batch is rigorously tested for harmful contaminants, heavy metals, allergens, and toxins' — and to third-party verification: 'Every formula undergoes independent third-party testing to confirm purity, potency, and label accuracy.' Every PDP reviewed repeats a 'Third-Party Tested' trust block ('Rigorously tested for quality and potency'). But no testing laboratory is named anywhere on the reviewed surface, no certificate of analysis is published or retrievable, and no lot or batch mechanism connects the claims to a specific tub. Probes of the common URL patterns (/pages/coa, /pages/lab-results, /pages/testing, /pages/quality, and equivalents) all return 404; the crawler's site-search queries for 'COA,' 'testing,' and 'lab' surfaced no additional pages; and the help center's four categories contain no testing or quality articles. The NASC certification statement is the one externally auditable quality signal, and it attaches to the company's quality system rather than to retrievable product test results.
The program stops one layer above buyer verification: no named laboratory, no published COA, no lot-level lookup anywhere on the brand surface. Naming the third-party labs and posting even representative batch COAs would lift the score to the 5–8 band; a lot-linked lookup would be required for 9–10.
Every formula undergoes independent third-party testing to confirm purity, potency, and label accuracy, ensuring the highest quality in every batch.
The quality system is named; the facilities are not. The About page states 'PetLabCo.® is NASC Certified, the gold standard in independent quality and safety certifications' and that products 'are manufactured in facilities that follow NASC, FDA, and cGMP guidelines, meeting the highest U.S. pet supplement standards.' A sitewide banner on every product page reads 'Manufactured In The USA from domestic & globally sourced ingredients,' and the About page locates formulation in the USA. Sourcing logic is partially disclosed: ingredients are 'vetted for potency and bioavailability, which means we analyze how and where ingredients are sourced and processed'; Green-Lipped Mussel is identified as New Zealand-sourced and non-heat-treated; and branded inputs carry supplier attribution on the label panels (AstaReal — Fuji Chemical Industries; Enzalox — Lallemand). Facility identity stays at country level: no facility name, city, or state appears anywhere in the reviewed surface, FDA status is framed as guideline adherence rather than explicit facility registration, and HACCP, SQF, and ISO are not referenced.
Disclosure matches the 8 anchor exactly: quality system named (NASC, cGMP, FDA guidelines) with facility identity held at country level. Naming co-manufacturing facilities at city/state level and stating FDA registration status explicitly would justify 9–10.
As an NASC-certified company, we ensure our products are manufactured in facilities that follow NASC, FDA, and cGMP guidelines, meeting the highest U.S. pet supplement standards.
The claim apparatus is dense and mostly disciplined. The home hero qualifies its lead claim inline — 'Our Advanced Dental Powder is clinically studied to reduce a bad breath-causing compound†' — with the dagger resolving on-page to the 28-day study description. Superlatives are footnoted to their actual basis ('America's #1 selling probiotic chew' resolves to 'YTD 2024 (as of Oct 31, 2024): PetLabCo.® PBC is #1 dog digestive remedy on Amazon'); results statistics are labeled as internal subscriber surveys with dates and sample sizes; product copy stays in structure-function register ('supports,' 'helps maintain,' 'occasional joint stiffness,' 'seasonal allergies') above a sitewide FDA disclaimer; and awards are footnoted to the granting body. Overshoot sits at the edges: the trademarked superlative 'Your Most Trusted Pet Health Optimization Partner™,' the unfalsifiable 'Just the science. No hyperbole. No unsupported health claims,' 'world's first clinically studied probiotic soft chews,' and learn-section article titles such as '7 simple hacks to end dog joint pain fast' and '8 natural ingredients proven to reduce joint pain' that run ahead of the structure-function discipline of the store pages. The post-purchase Getting Results page also repeats the 90-day study claim in prose without the PDP's footnote apparatus.
Learn-section headlines with treatment-strength phrasing, unfalsifiable trust superlatives, and footnote-free claim repetition on post-purchase pages sit alongside otherwise well-qualified commerce surfaces. Bringing editorial titles and secondary marketing pages into the same qualified register as the PDPs would support a 9.
Our Advanced Dental Powder is clinically studied to reduce a bad breath-causing compound
The About item in primary navigation expands to clearly titled destinations — Our Story (quality and testing commitments), Experts (the named advisory board), and Ingredients (the glossary) — putting three of the four evidence pillars within two clicks of the home page. PDPs carry anchor menus ('Vet Reviewed | Key Ingredients | Directions for Use | Product Benefits') that put dose panels, expert attribution, and footnoted claims one click deep from any product tile, and the home-page FAQ surfaces expert names and clinical-study scoping without any navigation at all. The Probiotic Chew finished-formula study does have a destination — a learn-section article documenting the study and its named author — but that article sits in the learn library rather than being linked from the Probiotic Chew PDP or primary navigation. What primary navigation still cannot reach is the testing artifact layer: there is no testing or COA page at any probed URL, the help center's four categories are commerce-only (subscriptions, shipping, returns, product usage), and manufacturing and testing evidence exist only as sections within the Our Story page rather than as dedicated linkable surfaces.
The testing pillar has no destination page, and the one published clinical study is reachable only deep in the learn library rather than linked from the product page or primary navigation. A consolidated trust hub linking study documents, laboratory identity, and COAs from primary navigation would push toward 9–10.
We believe informed pet parents make the best decisions. That’s why we provide science-backed resources to help you understand your pet’s health.
PetLab Co presents well above the DTC median on named-expert disclosure and claim qualification: a seven-member named advisory board with per-member scope of involvement, formul...
Front of the Pack pairs full per-active mg labeling on both supplements with an unusually well-cited ingredient-evidence catalog and a named, credentialed Chief Science Officer. The gaps are concentrated: finished-product testing is asserted but unverifiable (no named lab, no COA, no lot lookup), the manufacturing facility is held at 'Made in the USA', and 'clinically proven' marketing is applied at the formula level while the underlying studies are ingredient-level.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
What's in it
Full per-active milligram disclosure with no proprietary blends across both current SKUs — The One names all twelve actives with amounts and inactives, and Soothe names all five.
Public ingredient-evidence catalog citing studies with author lists, journals, years, study-design flags, and working links, each labelled as a dog, human, or review study.
One fully credentialed named expert, Dr. Jamie Peyton (DVM, DACVECC, CVA, CVC, CCRT), surfaced as Chief Science Officer with a dedicated bio page and verifiable qualifications.
What's not in it
No finished-product testing transparency: no named laboratory, no certificate of analysis, and no lot- or batch-level lookup — only an unquantified 'under the microscope eight separate times' claim.
Manufacturing is disclosed only as 'Made in the USA'; the facility is not named at facility/city/state level and no facility certification (NASC, cGMP, HACCP, FDA registration, SQF, ISO) is published.
Formula-level 'clinically proven' and 'Clinical Proof' language recurs on the home and product pages while the cited evidence is ingredient-level, with no statement that a finished-formula trial exists.
Why this score
itap any criterion for evidence
——
Why this score
What's missing
Brand's own words
Disclosure is near-complete and consistent across the current supplement line, which comprises two SKUs. The One publishes a 'Typical values per scoop' panel naming all twelve actives with per-active milligram amounts (krill 575mg, SunFiber guar gum 525mg, glucosamine 250mg, chondroitin 100mg, OptiMSM 100mg, taurine 100mg, curcumin phytosome 60mg, L-carnitine 50mg, BPL1 postbiotic 25mg, green tea extract 40mg, Sensoril ashwagandha 30mg, Suntheanine L-theanine 25mg), with serving size (~2g/scoop), a weight-based serving guide, a macronutrient table, and a named inactive-ingredients line. Soothe similarly discloses all five actives with per-active mg (MEG-3 fish oil 580mg, TruMune 250mg, Epicor 100mg, BiovaPlex egg membrane 50mg, Floradapt L. sakei 20mg). There are no proprietary blends and no grouped amounts anywhere in the line, and branded raw-material identifiers are named for nearly every active.
Two details hold this just below a clean 10: amounts are presented as 'typical values per scoop' rather than guaranteed label minimums with %DV in a formal Supplement Facts format, and Soothe's panel does not surface a separate inactive-ingredients line the way The One does. Publishing guaranteed minimums and a parallel inactives line on Soothe would close the gap.
Certified organic brown kelp (Ascophyllum nodosum), sea buckthorn (Hippophae rhamnoides [fruit]), silicon dioxide mineral source [stabilizer/carrier for L-carnitine].
The brand publishes ingredient rationale for both products and an explicit five-pillar selection framework on the Ingredients page (Clinically Proven, Pharma Purity, Canine-Centric, Consistency, Human-Grade), and groups actives by the body system they target (Active Body, Healthy Gut, Balanced Mind). Each active carries a short mechanism or role statement — for example, curcumin is described as operating 'as an antioxidant, defending against cellular damage and blocking the enzymes that cause inflammation', L-theanine as triggering serotonin and dopamine while 'stimulating calming alpha waves in the brain', and SunFiber as fermenting 'into short-chain fatty acids that help to cultivate good bacteria in the gut'. Most meaningful actives therefore have a stated biological role, and the Ingredients hub adds supplier-grade and absorption rationale per ingredient. Mechanism depth is uneven, however: several blurbs (ashwagandha, taurine) read closer to benefit lists than to mechanism, and each role statement is a single sentence.
The rationale is broad rather than deep — one sentence per active, with some actives described in benefit language rather than mechanism, and no criterion-by-criterion mechanism write-up tied inline to the cited study for every ingredient. Expanding each active to a fuller mechanism paragraph and linking it directly to its citation would lift this toward 9-10.
Curcumin operates as an antioxidant, defending against cellular damage and blocking the enzymes that cause inflammation in the body.
Citation infrastructure is a genuine strength. The /ingredients/evidence catalog presents 11 representative studies, each with title, full author list, journal, year, participant count, study-design flags (randomised / placebo-controlled / double-blind), and a working external link to PubMed, PMC, ScienceDirect, BioMed Central, ResearchGate, or CiteSeerX. Crucially, every study is labelled 'Dog', 'Human', or 'Review', so a buyer can immediately see that, for example, the L-carnitine and krill findings come from canine studies (56 Labradors; Iditarod sled dogs) while the chondroitin, MSM, and ashwagandha findings come from human trials. The limitation is the ingredient-versus-formula distinction: all cited studies are ingredient-level, none is on the finished 'The One' or 'Soothe' formula, and the page does not state that no finished-formula trial exists. The marketing surface then carries that ingredient evidence into formula-level claims — the home hero says ingredients are 'clinically proven to elevate your dog's whole-body health' and the PDP advertises '12 advanced ingredients with proven benefits in 400+ studies' under a 'Clinical Proof' header — without an inline qualifier that the proof is ingredient-level.
What holds this below 9-10 is that ingredient-level studies are presented in a finished-formula context on the home and product pages without explicit qualification, and the brand does not state openly that no study exists on the finished formula. Adding an above-the-fold qualifier that 'clinically proven' refers to ingredients, and a plain note that finished-formula trials have not been conducted, would move this up.
Our experts have assembled a catalog of 466 research publications verifying the health claims of our ingredients
The brand surfaces one fully credentialed named expert: Dr. Jamie Peyton, DVM, DACVECC, CVA, CVC, CCRT, identified as 'Chief Science Officer & Science Advisory Board Chair'. She is named with full post-nominals and a quote on the home page and the Ingredients page, and has a dedicated bio page listing her UC Davis emergency/critical-care residency, her ACVECC mentorship at Four Seasons Animal Hospital, and her 2019 UC Davis Chancellor's Innovation Award. This is substantive, verifiable veterinary disclosure rather than a placeholder. Two factors temper it: the expert is not reachable from primary navigation (there is no Experts or Team link; the dedicated page is found via a /experts redirect), and the About page — the natural team destination — describes only 'A team of vets, biochemists and dog lovers' without naming anyone. The 'Science Advisory Board' that Dr. Peyton chairs lists no other members anywhere on the site.
The score is held below 9-10 because the named expert is not surfaced from primary navigation and the About page anonymizes the team, and because the referenced advisory board has no other named members or roster. Linking the expert from the main nav, naming the rest of the board with credentials, and articulating each person's specific role would raise this.
Finished-product testing is asserted but not substantiated for buyers. The strongest statement is on the /info product pages: 'By putting all of our ingredients under the microscope not once, not twice, but eight separate times…' — an unquantified quality-control claim. No third-party laboratory is named anywhere on the site, no certificate of analysis or potency report is published, and there is no lot- or batch-level lookup tied to a specific bottle. Probing returned 404 for /testing, /quality, /lab-results, /third-party-testing, /coa, and /certificate-of-analysis, and a cross-page scan found no contaminant or microbial panel and no facility testing detail; the only GMP reference on the site belongs to the OptiMSM raw-material supplier, not to FOTP's finished products. The home-page badges ('Pesticide-free', 'Non-GMO') are unsourced brand statements rather than published test results.
The brand asserts testing but names no laboratory, surfaces no COA, and connects no testing to specific batches, which caps it at this tier. Publishing finished-product COAs with a named lab, a contaminant/microbial/potency panel, and a lot-linked lookup would move this up several tiers.
By putting all of our ingredients under the microscope not once, not twice, but eight separate times, we're hoping to raise the standards of quality control on the pet supplement industry. Once and for all.
Manufacturing disclosure is limited to a single element — a 'Made in the USA' badge in the home-page strip — with no facility named at facility/city/state level and no facility-level certification body cited (no NASC seal, cGMP, HACCP, FDA-registration, SQF, or ISO statement appears anywhere on the site). The brand does disclose meaningful ingredient sourcing on the Ingredients page: per-ingredient country of origin (krill from Norway, glucosamine and chondroitin from Spain, curcumin from Italy, several actives from India and Japan) plus supplier-grade rationale such as krill being 'The only MSC (Marine Stewardship Council) certified krill in the world, guaranteeing sustainable harvesting and traceability from the exact catch location'. The Sustainability page, which might host quality-system detail, is packaging-only. So sourcing logic is real at the ingredient level while the assembly facility and its quality system remain undisclosed.
The facility is not identified and no facility-level quality system (NASC, cGMP, HACCP, FDA registration, SQF, ISO) is disclosed, which holds the score at the single-element tier despite strong ingredient-sourcing detail. Naming the manufacturing facility and its certifications would lift this to 8 and above.
The only MSC (Marine Stewardship Council) certified krill in the world, guaranteeing sustainable harvesting and traceability from the exact catch location
The brand avoids disease-treatment and cure language, and its clinical-style claims are backed by a real, publicly linked ingredient-evidence catalog rather than resting on unsupported assertion — meaningful discipline that keeps it well clear of the lower tiers. The mix is uneven, though, on formula-level certainty. The home hero states ingredients are 'clinically proven to elevate your dog's whole-body health', the PDP advertises '12 advanced ingredients with proven benefits in 400+ studies' under a 'Clinical Proof' header, and the site promises 'Real Results: Visible improvements within 6 weeks, or it's on us'. Because the underlying evidence is ingredient-level and no finished-formula trial is disclosed, this formula-level 'clinically proven / Clinical Proof' framing recurs across the home and product surfaces without an inline qualifier. The hero's specific wording — 'ingredients clinically proven' — is a partial qualifier, but the broader pattern asserts whole-product proof the brand's evidence supports only at the ingredient level.
Recurring formula-level 'clinically proven' / 'Clinical Proof' language and a results guarantee outrun an ingredient-level evidence base, which holds the score at the mixed tier. Qualifying clinical claims as ingredient-level above the fold, and softening whole-product certainty where no finished-formula trial exists, would raise it.
Try The One (and only) supplement with ingredients clinically proven to elevate your dog's whole-body health.
Of the four trust pillars, the science pillar is the most navigable: 'Ingredients' sits in the primary navigation, and the full evidence catalog with authors, journals, and study links is one step further at /ingredients/evidence — genuinely strong, inspectable, pre-purchase evidence. The other pillars are harder to reach or thin. The named expert, Dr. Jamie Peyton, is quoted on the home and Ingredients pages but her credentialed bio page is not linked from primary navigation and the About page anonymizes the team. Testing has no destination page (only the unquantified 'eight separate times' line buried on the /info product pages), and manufacturing is a single home-page badge — so two pillars cannot be inspected in three clicks. There is no consolidated trust hub tying science, testing, experts, and manufacturing together.
Science is easy to reach, but the expert page is outside primary navigation, the About page is anonymous, and testing and manufacturing lack any findable destination, so a buyer cannot inspect all four pillars in three clicks. A consolidated trust hub plus nav links to the expert and a testing page would raise this.
Most dog supplements rely on generic ingredients and anecdotal claims. We're taking the opposite approach, to guarantee that all of our ingredients are backed by verifiable research publications.
Front of the Pack pairs full per-active mg labeling on both supplements with an unusually well-cited ingredient-evidence catalog and a named, credentialed Chief Science Officer....
Only Natural Pet names a credentialed holistic veterinarian and publishes lot-linked, Eurofins-tested Certificates of Analysis for its CBD/hemp sub-line, but that testing coverage and its formal quality-system certificat
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreePublic COA LookupPer-Lot TraceabilityNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
A single named veterinarian, Dr. Jean Hofve, DVM, is fully credentialed on a dedicated bio page reachable within about three clicks of the homepage via primary navigation.
Real, lot-numbered Certificates of Analysis from the named third-party lab Eurofins are publicly posted and were independently verified by decompressing a sample PDF.
Nearly every active ingredient across the supplement line is disclosed with an exact per-serving mg or enzyme-unit amount, with only the flagship product's probiotic strains grouped into one blend figure.
What's not in it
The verified Certificate-of-Analysis program covers only the CBD/hemp sub-line (about 7 of roughly 104 house-brand SKUs) and is not linked from primary navigation or any product page — it is discoverable only via sitemap.
No manufacturing facility name, city, or state was found anywhere in the pages read in this pass, and no cGMP, HACCP, FDA-registration, or ISO-certification language was found on any page.
No PubMed ID, DOI, journal name, or other citation was found anywhere in this pass, including on the one article with a named, credentialed author.
Only Natural Pet names a credentialed holistic veterinarian and publishes lot-linked, Eurofins-tested Certificates of Analysis for its CBD/hemp sub-line, but that testing covera...
VetriScience presents above the category median on label disclosure and manufacturing identity: full Product Facts images on every PDP reviewed, an owned SQF-certified FDA-registered Vermont operation, and founding NASC membership. Its clinical posture is distinctive — four finished-product studies described in methodological detail — but the storefront does not link them; the full write-ups (named investigators, and a companion analysis published in the Journal of Medical Science, 2008) live in a separate brand library that is not linked from the consumer surface and currently behind an expired certificate. The remaining gaps are artifact-level: no named testing laboratory, no public COA or lot lookup, and no named formulator behind the line's vet-formulated identity.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
What's in it
Complete back-of-pack Product Facts panels are published as gallery images on every PDP reviewed, quantifying every active in mg/IU/CFU — including strain-level probiotic identification (Bacillus coagulans GBI-30, 6086) and a 28-line senior multivitamin panel.
Finished-product clinical work is described with real methodological detail — a randomized double-blind crossover study at Washington State University, two CanCog Technologies calming studies, and a 20-dog VOHC-scored dental trial — rather than borrowed ingredient research.
Manufacturing disclosure pairs facility ownership with named regimes: products are made in the brand's own SQF-certified, FDA-registered Vermont facilities under cGMP, with founding membership in NASC documented on a dedicated page.
What's not in it
The four clinical studies are described on the storefront with no inline citation or link; the full write-ups — with named investigators, and a companion analysis published in the Journal of Medical Science (2008) — sit in a separate info.vetriscience.com white-paper library that is not linked from the consumer surface and currently behind an expired security certificate, so a buyer cannot reach a citable study from the site.
No certificate-of-analysis access exists at any depth — no named third-party laboratory, no lot-level lookup, and no disclosed contaminant or microbial panel scope, with eleven probed COA-style URLs returning 404.
'Vet Formulated. Pet Approved.' appears on every label, but no formulator is named; the credentialed veterinarians on the VetriExperts page are surfaced as consultants and ambassadors, not as the people who designed the formulas.
VetriScience presents above the category median on label disclosure and manufacturing identity: full Product Facts images on every PDP reviewed, an owned SQF-certified FDA-regis...
PetHonesty scores above the DTC median on named experts, numeric label panels, and quality-system naming: six credentialed advisors are published, every reviewed product carries per-active amounts, and GMP / FDA-registered / SQF / NASC disclosures are specific. The gaps cluster on verification artifacts — no COA access or named laboratory, citations confined to joint ingredients on an unlinked Sources page, an empty Our Research page, and a comparative 'Real Results' campaign that outruns the published evidence base.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
What's in it
Six named experts with disclosed credentials — including a DACVIM board-certified internist and an in-house PhD Chief Scientific Officer whose formulator role is corroborated on three separate pages — reachable from primary navigation.
Standardized numeric Guaranteed Analysis / Active Ingredients panels with per-active mg, IU, and CFU amounts on every reviewed product across chews, powders, oils, and the cat line.
Quality-system disclosure names five distinct elements in one FAQ answer — U.S.A. manufacture, GMP certification, FDA registration, SQF, APHIS — plus the NASC quality seal.
What's not in it
No public COA library, lot lookup, or named third-party laboratory exists anywhere on the site; testing language stays at 'rigorously tested' with one unattributed '3rd party tested' card on the fish oil page.
Published citations cover only joint/mobility ingredients, the Sources and References page is not linked from any navigation surface, and the page titled 'Our Research' carries no content at review time.
Manufacturing facility identity is held at country level ('made in the U.S.A.') with no facility name, city, or state, and Allergy Support's seven-mushroom proprietary blend discloses a 100 mg total without per-species amounts.
PetHonesty scores above the DTC median on named experts, numeric label panels, and quality-system naming: six credentialed advisors are published, every reviewed product carries...
Nordic Naturals Pet gives buyers a public testing and quality trail centered on a lot-linked COA pathway, a named Norway manufacturing facility (Nordic Pharma), an NASC-audited facility relationship, and fish-oil sourcing certifications. A second production step (Southern California bottling/encapsulation) and an NSF-specific facility certification are disclosed but remain single-sourced without independent corroboration. Current expert roles, complete official-page text labels for the soft-chew line, pet-specific sample COAs, and named testing laboratories are not all surfaced from a buyer-verifiable hub.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
What's in it
The Nordic Promise and product pages give buyers a lot-linked COA pathway with potency, purity, and freshness framing.
Nordic Naturals names its primary fish-oil manufacturing facility (Nordic Pharma, Tromso, Norway) on its own site and has passed an independent NASC facility audit with Quality Seal permission, alongside Friend of the Sea and third-party non-GMO sourcing certifications.
The pet microsite and Q&A PDF provide omega-3 rationale, a named veterinary nutrition author, and study citations, though the citation set and author byline are dated to 2010.
What's not in it
The named veterinary nutrition expert is surfaced only in a 2010-dated educational PDF and does not appear on any current (2026) Nordic Naturals pet page checked.
The official joint, skin, and digestive soft-chew product pages do not publish numeric supplement-facts or guaranteed-analysis panels in accessible text; the per-mg figures are reachable only via a third-party retailer page.
Current product pages use research-backed phrasing without linking each claim to finished-formula study metadata, and no third-party testing laboratory or NSF-specific facility certification is independently corroborated on any reachable page.
Nordic Naturals Pet gives buyers a public testing and quality trail centered on a lot-linked COA pathway, a named Norway manufacturing facility (Nordic Pharma), an NASC-audited ...
YuMOVE discloses every active by dose across its joint line and footnotes its claims to named studies and surveys, including a finished-formula Royal Veterinary College trial that is summarized as data-on-file rather than a published, linked study. A named, credentialed veterinary and R&D team is published on the US surface, but only on a deep page that primary navigation does not link to. Remaining gaps cluster on testing and manufacturing identity: there is no named laboratory, no public COA or lot lookup, and manufacturing is disclosed only as 'made in the USA' without a facility name or quality-system certification.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Evidence Buried
The brand technically publishes meaningful science, evidence, testing, or expert disclosure, but buyers cannot reach it without dedicated effort. Evidence that exists but is hard to find counts less.
What's in it
The modal joint line publishes full per-active mg panels with no proprietary blend, from Glucosamine HCl 500mg and Green Lipped Mussel Powder 300mg on the Soft Chews to an eight-active panel on the PLUS tablets.
A dedicated Research & Studies page distinguishes a finished-formula Royal Veterinary College RCT (40 dogs, double-blind, placebo-controlled crossover) from ingredient-level evidence and provides downloadable peer-reviewed papers for Green Lipped Mussel, N-acetyl-D-glucosamine, and Hyaluronic Acid.
Marketing claims are consistently footnoted to named, dated sources and a non-disease disclaimer, with an Our Claims page mapping each headline statement to its survey or study.
What's not in it
No public finished-product testing program: no named third-party laboratory, no contaminant, microbial, or potency panel for the finished product, and no certificate-of-analysis or lot-number lookup (probed COA and testing URLs return 404).
The primary 'Our Story' page names only co-founder Dr. John Howie with no stated credentials; the named, credentialed veterinary and R&D roster (four of five holding MRCVS) appears only on The Lintbells Story page, which primary navigation and the footer do not link to, so a buyer reaches it only via on-site search or direct URL.
Manufacturing is held at country level ('now manufactured in the USA using globally sourced ingredients') with no facility name, city, or state and no quality-system certification (NASC, cGMP, FDA-registration, HACCP, SQF, or ISO).
YuMOVE discloses every active by dose across its joint line and footnotes its claims to named studies and surveys, including a finished-formula Royal Veterinary College trial th...
Honest Paws operates one of the few buyer-usable batch-linked COA lookups in the DTC pet CBD segment, with full contaminant panels from a named ISO 17025-accredited laboratory, and publishes exact CBD doses across its hemp line. Disclosure weakens off that flagship line: non-CBD products sit outside the COA tool and several omit per-active amounts, veterinary claims are not tied to named experts, and manufacturing identity stays at country level.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreePublic COA LookupPer-Lot TraceabilityNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Batch-linked Certificates of Analysis lookup covering 26 CBD product types and 154 batches, serving full-panel PDFs — cannabinoid potency, pesticides, mycotoxins, residual solvents, heavy metals, and microbiology — from SC Laboratories, an ISO 17025-accredited laboratory named on every report.
CBD-line label disclosure is consistent and exact: every bite, soft chew, and tincture strength publishes hemp-oil mg with naturally occurring CBD mg per serving, plus itemized inactives and weight-banded feeding charts.
NASC Quality Seal disclosure goes beyond the badge — a dedicated page documents biennial third-party audits, adverse event reporting, a Quality Control Manual, and GMP adherence, and PDPs identify the brand as an audited NASC Primary Supplier Member.
What's not in it
Veterinary involvement is asserted sitewide ('Vet Recommended', 'Veterinarian-reviewed') but never connected to a named individual; the DVM bios that exist are unlinked team pages that state no formulation, review, or advisory role.
The non-CBD line discloses materially less than the CBD line: no non-CBD product appears in the COA lookup, the Multivitamin and Omega-3 Fish Oil publish no per-active amounts, and Probiotics and Turkey Tail hold part of their panels at blend-level totals.
Manufacturing identity is held at country level — 'USA made' with GMP and NASC language but no facility name, city, or state, and no FDA facility-registration disclosure.
Honest Paws operates one of the few buyer-usable batch-linked COA lookups in the DTC pet CBD segment, with full contaminant panels from a named ISO 17025-accredited laboratory, ...
A hemp brand that refuses the CBD ambiguity — no cannabinoids, THC-absence testing, Canadian VHP claim review — co-founded by a named Doctor of Veterinary Medicine, with region-level manufacturing disclosure and an ingre
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
What's in it
A named, fully credentialed co-founder veterinarian (Dr. Daniela Fischer, DVM/MSc/PhD) is disclosed on both the homepage and the primary-nav ingredients page, with a stated role overseeing product formulas.
Rare hemp honesty — 'Our products don't contain any cannabinoids' — with THC-absence testing stated, external claim review via the Canadian Veterinary Health Product designation, and NASC regulations followed in the US.
Full per-active mg panels with no proprietary blends were confirmed across five checked SKUs spanning three of the four product families, plus region-level manufacturing disclosure (British Columbia and Alberta) and named Saskatchewan hemp sourcing.
What's not in it
The described ingredient-COA program is unpublished: no named lab, no public certificate, no lot access, confirmed across all 15 archived pages and direct handle probes for common COA/quality-page URLs.
Four of four calming-line product pages checked use unqualified 'clinically studied'/'clinically researched' language with no study, author, or journal surfaced anywhere on the reviewed surfaces.
No facility name, street address, or city/state-level manufacturing location is disclosed (province-level only), and no cGMP, HACCP, FDA-registration, SQF, or ISO certification appears on any reviewed page.
A hemp brand that refuses the CBD ambiguity — no cannabinoids, THC-absence testing, Canadian VHP claim review — co-founded by a named Doctor of Veterinary Medicine, with region-...
Virbac is a sourceable veterinary-channel brand with stronger dental evidence signals than many supplement brands, especially through VOHC, and a named credentialed veterinarian and quality/compliance officer in public leadership bios. The buyer still has to assemble label detail, manufacturing geography, and expert roles from several disconnected public sources, and lot-level testing evidence remains unpublished.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
What's in it
VOHC acceptance gives the C.E.T. dental line a buyer-visible external dental-claim signal, and one veterinary product page publishes a 4-item numbered study reference list.
Public pages disclose headquarters, a St. Louis-area manufacturing facility, and a named Vice President whose role covers FDA and worldwide GMP compliance.
A named, fully-credentialed veterinarian (Dr. Alan Taylor, holding a Bachelor's degree in Veterinary Medicine and Surgery from the University of Glasgow) is surfaced in primary navigation, though not tied to the C.E.T. line by name.
What's not in it
Full active-by-active amounts are not consistently published on official product pages.
No buyer-facing lot-level COA lookup or named laboratory panel was surfaced despite dedicated sitemap and common-handle probing.
The named veterinarian's and quality officer's disclosed scope covers Virbac North America broadly, not the C.E.T. supplement or dental line specifically, and one product page's footnote citation numbering does not resolve to its reference list.
Virbac is a sourceable veterinary-channel brand with stronger dental evidence signals than many supplement brands, especially through VOHC, and a named credentialed veterinarian...
Dover, Delaware (registered address; manufacturing facility not disclosed)
66/100
as of 2026-07-03
Disclosure Gaps
VitaDog has a real editorial-policy spine, a substantive peer-reviewed sources page, named third-party testing, and a named (if country-level-only) manufacturing quality standard — but the badge stack (Vet Reviewed, Clinically Dosed, Public Eurofins COAs) overpromises against the underlying surface. The testing panel is microbiology-only on one SKU, the brand's own 'vet-led advisory board' has no named members even though an unrelated named DVM appears elsewhere as a third-party endorser, no finished-formula trial exists, and no manufacturing facility is named. Stronger than the median DTC peer on editorial-policy and quality-system scaffolding; weaker than the marketing implies on named-expert substance.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Publishes a substantive 41-entry peer-reviewed sources library with PubMed IDs and DOIs, verified in full against the live page (41 PMIDs, 41 PubMed links, 36 DOIs).
Issues a real editorial policy with three-tier evidence grading and an explicit admission that the founder-reviewers are not DVMs.
Names Eurofins (ISO/IEC 17025:2017) as testing partner and publishes two per-lot COA PDFs, plus names cGMP as its manufacturing quality standard.
What's not in it
Eurofins COAs cover microbiology only (E. coli, Salmonella, Yeast, Mold) — no heavy metals, no pesticides, no potency on actives disclosed in the published COAs.
The brand's own 'vet-led advisory board' and formulation-review claims do not name any individual; a named DVM does appear sitewide, but in a third-party testimonial capacity (Chief Veterinary Officer at an external animal shelter) rather than as VitaDog's own formulator or reviewer.
No manufacturing facility name, city, or state is disclosed anywhere on the site; disclosure stops at 'US-based facility' plus the named cGMP standard.
VitaDog has a real editorial-policy spine, a substantive peer-reviewed sources page, named third-party testing, and a named (if country-level-only) manufacturing quality standar...
Bernie's Perfect Poop discloses per-active doses across its core supplements and backs ingredients with a genuine 23-study research library and mechanism content — stronger evidence work than most Amazon-native challengers. The gaps are structural rather than in product copy: no named veterinarian, no inspectable certificate of analysis or named testing lab, and manufacturing certified (cGMP, SQF) but never named at facility level. Evidence is also split across three brand domains with no single trust hub.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Evidence Buried
The brand technically publishes meaningful science, evidence, testing, or expert disclosure, but buyers cannot reach it without dedicated effort. Evidence that exists but is hard to find counts less.
What's in it
Per-active dose disclosure across the core supplement line — Perfect Poop lists each fiber, prebiotic and probiotic amount, and Marvelous Mobility and Healthy Hips itemize all 16 actives in mg/mcg with no proprietary blend.
An unusually deep ingredient-research presence for the category: a 'University' library of 23 studies cited with authors, journals and links, paired with mechanism-level rationale on the Perfect Poop ingredients page.
Disciplined claim language — PDPs avoid 'clinically proven', carry the standard non-disease disclaimer, and qualify the headline '5X DHA+EPA' claim with a stated label-comparison methodology.
What's not in it
No veterinarian is named anywhere; the products' veterinary and formulation expertise is described as an unnamed 'Ph.D. veterinary science researchers' partnership, with only educational/R&D staff (Emily Halaszynski, Vince) surfaced by name.
Testing is asserted as a badge ('External third-party lab testing') but is not verifiable: no laboratory is named, no certificate of analysis is published, and probed COA-lookup URLs all return 404.
Manufacturing identity is held at country level only — cGMP and SQF certifications are named, but no facility name, city, or state and no ingredient-sourcing detail are disclosed.
Bernie's Perfect Poop discloses per-active doses across its core supplements and backs ingredients with a genuine 23-study research library and mechanism content — stronger evid...
Nutramax Laboratories discloses more about doses and manufacturing than most of the category: complete per-active panels on flagship PDPs, an owned Lancaster, SC manufacturing campus, and consistently footnoted marketing superlatives. Its gaps are verification artifacts — no public COA or lot lookup, no named third-party lab, study claims cited publicly only on the Denamarin About page, and no named formulating experts — with the deeper research record gated behind its veterinary portal.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Evidence Buried
The brand technically publishes meaningful science, evidence, testing, or expert disclosure, but buyers cannot reach it without dedicated effort. Evidence that exists but is hard to find counts less.
What's in it
Per-active dose disclosure is complete on the flagship joint and liver lines, down to branded-ingredient identity (FCHG49 glucosamine, TRH122 chondroitin) and delivered silybin (24 mg Silybin A+B), with strain-level NCIMB identifiers on the probiotic.
Vertically integrated manufacturing is disclosed past the category norm: Nutramax-owned facilities in Lancaster, South Carolina, with a published eight-step quality process, in-house Chemistry and Microbiology labs, and a label-claim guarantee.
Claim qualification is unusually consistent — every '#1 Veterinarian Recommended' superlative across all reviewed domains carries a survey-source footnote, and product copy stays inside structure/function language.
What's not in it
No public COA, lot lookup, or named third-party laboratory exists anywhere on the surface — the detailed testing program is entirely self-attested and in-house, with contaminant panels never itemized.
Clinical-style claims outrun their public citations: Proviable's '6 published studies in dogs and cats' and 'Clinically Researched' badge carry no reference list, and Dasuquin's comparative research claim discloses its cell-culture basis only in fine print.
No formulating veterinarian, scientist, or advisory board is named at product level; the only named DVM is the President & CEO, visible solely in media-center press releases, while the research library is login-gated to professionals.
Nutramax Laboratories discloses more about doses and manufacturing than most of the category: complete per-active panels on flagship PDPs, an owned Lancaster, SC manufacturing c...
Strong on clinical evidence and named veterinary involvement, weak on label disclosure and testing. The brand publishes one of the most credible pieces of evidence in the pet-supplement category — a peer-reviewed finished-formula RCT at NC State CVM — and surfaces a real veterinary team. But buyers cannot identify the specific NAD precursor or senolytic compound in the product, cannot retrieve a lot-specific COA, and cannot find the manufacturing facility by name, city, and state. The result is an unusually clinical-evidence-forward brand sitting on top of a conventional pet-supplement label / testing / facility disclosure layer.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
What's in it
Published finished-formula RCT of the Leap Years product itself — double-blind, placebo-controlled, conducted at North Carolina State University College of Veterinary Medicine, peer-reviewed in Scientific Reports (Nature Portfolio, May 2024) with Dr. Natasha Olby (DACVIM Neurology) as principal investigator.
Multiple DVMs publicly named with full credentials and state of practice, including internal scientific leadership (Dr. Ginny Rentko, VMD, DACVIM, Chief Veterinary Medical Officer) and the trial PI (Dr. Olby) plus seven independent practitioner commentators — well above the pet-supplement floor of 'our veterinary team.'
Disease-treatment claims are avoided; clinical-style language ('Clinically tested,' 'Studied in Dogs') is anchored to a real trial that buyers can read at nature.com, not to a phantom study.
What's not in it
Active ingredients are not named at the chemical level — the brand discloses 'NAD Booster' (200mg / 600mg) and 'senolytic' as functional categories, confirms the product does not contain NMN, but never tells the buyer which precursor (NR, NAR, NA) or which senolytic compound (fisetin, quercetin, etc.) is in the formula.
Testing disclosure is generic: no named third-party laboratory, no public COA lookup, no per-lot traceability, no itemized contaminant / microbial / pesticide / potency panel.
Manufacturing facility is not named at the facility-name / city / state level; sourcing is described as 'globally sourced ingredients' with no named suppliers or countries of origin.
Strong on clinical evidence and named veterinary involvement, weak on label disclosure and testing. The brand publishes one of the most credible pieces of evidence in the pet-su...
Finn presents above the DTC median on label transparency: all six core soft-chew supplements publish per-active doses with no proprietary blends beyond grouped probiotic CFU totals. Manufacturing is disclosed at quality-system level (cGMP, SQF, NASC) and batch microbial testing is described organism-by-organism. The gaps cluster on verifiability — no named laboratory, no public COA, no cited studies behind 'clinically proven' language, and no named formulator — with most quality content held in the brand's help center rather than primary navigation.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreePublic COA LookupPer-Lot TraceabilityNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
What's in it
Complete per-active dose disclosure across all six core soft-chew supplements — from Organic Passion Flower 125 mg on Calming Aid to Glucosamine HCL 500 mg on Hip & Joint — with defined per-chew serving sizes, weight-based dosing charts, and on-page inactive ingredient lists.
Quality-system disclosure names three frameworks (cGMP compliance, SQF certification, NASC Quality Seal via third-party audit) and the batch testing description names its microbial panel organism-by-organism (Salmonella, Listeria, Enterobacteriaceae) with lot-code traceability.
Three veterinarians are named with credentials directly on the home page (Dr. Laura Robinson, DVM; Dr. Kerri Nelson, DVM, PGRS-C; Dr. Farren Billand, DVM), and core PDP claim language stays consistently qualified ('helps occasional stiffness,' 'supports calm').
What's not in it
No third-party laboratory is named and no COA or lot-lookup is published — every-batch testing and traceability codes are described in help-center text, but no testing document is buyer-accessible.
'Clinically proven' and 'selected based on clinical research' statements carry no citation anywhere on the reviewed surface — no study, author, or journal is identified, and no science or research page exists on the site.
Manufacturing, testing, and sourcing detail lives only in the footer-linked Gorgias help center rather than the primary site; the facility is identified at country level only, and the named DVMs' published role is limited to endorsement quotes with no disclosed formulator.
Finn presents above the DTC median on label transparency: all six core soft-chew supplements publish per-active doses with no proprietary blends beyond grouped probiotic CFU tot...
Open Farm's transparency strength is operational and personnel-based: sourcing, ingredient origins, lot-code traceability, and a named, credentialed veterinary nutritionist are all publicly disclosed, though the nutritionist's role is described for the food line rather than the supplement line specifically. It is less transparent as a supplement clinical-evidence system because supplement-specific study citations, named testing laboratories, and facility-level manufacturing detail were not found in the pages reviewed, even though the brand discloses honestly that it has not yet published peer-reviewed recipe research.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreePublic COA LookupPer-Lot TraceabilityNASC MemberFinished-Formula TrialNamed Mfg Facility
What's in it
The site publishes a prominent lot-code traceability system for ingredient origins and deeper product information.
A named, credentialed in-house veterinary nutritionist (Dr. Moran Tal-Gavriel, DVM, DVSc, Dip. ECVCN) is disclosed with a described role on the FAQ page.
Two sampled supplement PDPs (Skin & Coat, Probiotic Chews) both publish quantified guaranteed-analysis values and ingredient-origin details.
What's not in it
The named veterinary nutritionist's role is described for Open Farm's food recipes generally rather than the supplement line specifically, and is disclosed only inside an FAQ accordion rather than a dedicated expert page.
No supplement-specific clinical citations, study library, or finished-formula trial disclosure was found; the brand does disclose that it has not yet published peer-reviewed recipe research.
Manufacturing facilities are disclosed only at the country level (United States, Canada, Iceland), with no named facility, city, state, or specific quality-system certification (NASC, cGMP, HACCP, FDA registration, SQF, ISO).
Open Farm's transparency strength is operational and personnel-based: sourcing, ingredient origins, lot-code traceability, and a named, credentialed veterinary nutritionist are ...
Verified transparency record for Adored Beast Apothecary, completed 2026-07-03. All 14 cited sources were fetched and archived; every exact_quote was confirmed verbatim against its cited source; the brand's own site was actively probed for COA, facility, and named-expert pages before any score reflecting an absence was finalized. Named-expert and scientific-rationale evidence are strong and easy to find; testing/COA and manufacturing disclosure are the brand's weakest areas.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
Founder and formulator Julie Anne Lee, DCH RCSHom is named with full credentials and biographical detail on a page linked directly from the site's primary top-level navigation.
The flagship Healthy Gut and the Equine and Feline Gut Soothe formulas publish full per-active mg/CFU dose panels rather than a single blended total.
A dedicated Ingredient Glossary explains a biological mechanism, not just a benefit claim, for most of the roughly 50 actives used across the line.
What's not in it
No public, lot-linked certificate-of-analysis lookup, named third-party laboratory, or contaminant/microbial/potency panel was found anywhere on the site; certificate-of-analysis access is described as available to professional buyers working directly with the manufacturer, not the public.
No manufacturing facility name, city, state, or quality-system certification (NASC, cGMP, HACCP, FDA registration, SQF, ISO) is disclosed; the only manufacturing claim found is a country-level "Handcrafted in the USA" banner.
Several products (Canine Gut Soothe, Gut Soothe, and the Liver Tonic component sold inside both protocol bundles) label part of their formula a proprietary blend with a total CFU or no per-active amount, while the flagship and other SKUs disclose full per-active dosing.
Verified transparency record for Adored Beast Apothecary, completed 2026-07-03. All 14 cited sources were fetched and archived; every exact_quote was confirmed verbatim against ...
67 Victoria Street East, PO Box 10007, New Tecumseth, Ontario L9R 1L5, Canada
63/100
as of 2026-07-03
Disclosure Gaps
Verified transparency record for Four Leaf Rover, current as of the 2026-07-03 hostile adversarial verification pass. All 13 cited sources were independently fetched and archived; all 8 rubric criteria carry score_status 'verified' with evidence, exact quotes, gaps, confidence levels, and source references checked against the tier ladders.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
A named formulator (Dr. Patricia Jordan) and NASC membership with independent third-party audit language are disclosed on the Our Story page.
The home page's Trust & Transparency section discloses a GMP-compliant Texas manufacturing plant and an on-request testing-results offer without requiring footer navigation.
Genuine named-compound ingredient-mechanism content (not just benefit language) appears on 3 of 9 product pages, including two specific third-party-verified potency-percentage guarantees on Seven Shrooms.
What's not in it
No page in the reviewed set shows a text-readable per-active mg/mcg/IU dose panel or serving size, and the site's own 'Guaranteed Analysis' accordion component was not found populated with visible numeric content on any archived page.
No finished-formula clinical citation, named third-party testing laboratory, or public COA lookup was found anywhere across 13 archived pages.
The named formulator's credential scope stays vague (no bio page, license detail, or explicit scope-of-involvement statement), and the page that names her sits outside primary navigation.
Verified transparency record for Four Leaf Rover, current as of the 2026-07-03 hostile adversarial verification pass. All 13 cited sources were independently fetched and archive...
Verified research record for Glandex following a full adversarial pass on 2026-07-03. All 8 rubric criteria were re-scored against the tier ladder anchors using freshly archived source pages; every exact_quote was confirmed verbatim against its cited source, and absence claims for named experts, testing, and manufacturing disclosure were actively probed via sitemap and direct-handle checks before being accepted or refuted.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Closed Science
The brand publishes strong testing or COA evidence but does not surface ingredient rationale, named experts, or finished-formula evidence. Testing alone is not enough to make the science verifiable.
What's in it
The flagship Soft Chews and both powder SKUs disclose all 8 active ingredients with per-serving mg or CFU amounts and no proprietary blend.
A real, primary-nav-linked Vet Advisory Board page names over a dozen credentialed veterinarians, including the brand's founder, who is also credited as the About Glandex page's named medical reviewer.
Ingredient rationale (fiber mechanism, anti-inflammatory pathway, gut-microbiome support) is explained consistently across the entire product line, not just the flagship.
What's not in it
An unqualified 'clinically proven' phrase appears identically on every Glandex product page with no study, ingredient name, or citation attached, and the site's own dedicated study-citation page covers a different product line (YuMOVE), not Glandex.
No testing or COA program is published anywhere on the site; direct probes of common testing-page handles all returned 404, and no lab, contaminant panel, or lot traceability is named.
Manufacturing disclosure names FDA registration and cGMP compliance but does not name a facility, city, or state anywhere in the published pages.
Verified research record for Glandex following a full adversarial pass on 2026-07-03. All 8 rubric criteria were re-scored against the tier ladder anchors using freshly archived...
The Missing Link has one of the better buyer-facing label paths among the remaining brands, across both powders and chews, and discloses NASC certification and FDA facility registration on its Amazon listing. Its main gaps are lot-level testing records, clinical citation transparency, and current expert review beyond the founder story.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
What's in it
Most representative products across powders and chews publish directions, ingredients, and per-active mg amounts.
The brand publicly names founder and veterinarian Dr. Robert Collette on its About Us page.
NASC certification and FDA facility registration are disclosed on the brand's Amazon listing, alongside made-in-USA and cold-processing language.
What's not in it
No public COA lookup, named lab, or lot-specific report was found.
Proof-oriented claims recur across multiple pages without visible study documentation.
Current expert-review scope beyond the founding story is not mapped to each formula.
The Missing Link has one of the better buyer-facing label paths among the remaining brands, across both powders and chews, and discloses NASC certification and FDA facility regi...
Rebuilt research record for Super Snouts from live-fetched surfaces (2026-07-03): homepage, FAQ, the informatives COA library, product pages, and — added during adversarial verification — a second COA page (Test Results) and an education page (CBD 101) discovered via sitemap and navigation inspection. Every rubric item carries verified evidence, a verbatim quote, gap, and confidence level.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Two public, lot-numbered COA archives covering raw-material and finished-product third-party verifications for the CBD/hemp line — one organized by product category (25 named groups), one chronological — naming a testing lab (KND Labs) directly in-document.
A real, independently-verified safety citation: the informatives page cites a peer-reviewed veterinary toxicology paper (PMID 23796481) to support its non-detectable-THC standard, honestly scoped to the safety claim rather than borrowed for efficacy.
Single-ingredient transparency at its best: Joint Power is '100% New Zealand Green Lipped Mussel' with weight-based dosing and loading-phase guidance; a dedicated CBD 101 page explains the water-soluble absorption mechanism in structured, buyer-facing terms.
What's not in it
No named individual anywhere: veterinary direction is attributed to an unnamed supplier expert AND a separately-claimed, unnamed in-house 'Chief Veterinary Officer'; 'Veterinary recommended' badges carry no name either.
6 of 8 reviewed non-CBD products name every ingredient but publish no per-active amounts; Super Shrooms uses explicit 'Proprietary Blend' labeling for its 7 mushroom actives.
The two COA archives cover the CBD/hemp product line only — none of the 8 non-CBD products reviewed for other criteria (Joint Power, Firm Up, G.I. Balance, Lion's Roar, Pumpkin Latte, Super Shrooms) appear in either archive — and the archives are not cross-linked to each other.
Rebuilt research record for Super Snouts from live-fetched surfaces (2026-07-03): homepage, FAQ, the informatives COA library, product pages, and — added during adversarial veri...
Tomlyn (Vetoquinol USA) discloses NASC membership and two named, credentialed veterinarians, but only on pages outside primary navigation, and publishes no per-active dose panel, laboratory name, or COA anywhere on its f
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Evidence Buried
The brand technically publishes meaningful science, evidence, testing, or expert disclosure, but buyers cannot reach it without dedicated effort. Evidence that exists but is hard to find counts less.
What's in it
Two named veterinarians (Dr. Jim Lowe, DVM and Dr. Jim Spiezio) are publicly documented, with Dr. Spiezio stating direct involvement developing specific Tomlyn products.
A real, verifiable published citation (Stiles et al., 2002, American Journal of Veterinary Research) is footnoted directly to a specific claim on the L-Lysine product page, and NASC membership is stated with an audit requirement on the About Us page.
The L-Lysine product carries a genuine active-ingredient-per-dose panel with inactive ingredients listed separately and clear per-life-stage directions.
What's not in it
No laboratory, certificate of analysis, or lot-lookup exists anywhere on the site — confirmed via direct probes of eleven common transparency-page handles, all returning HTTP 404.
The four-SKU Nutri-Cal flagship line lists ingredients without any per-active mg/IU amounts, unlike the brand's own L-Lysine product.
The named-veterinarian bios and the product-specific citation are reachable only via direct blog URLs or site search — the brand's own confirmed primary navigation has no science, testing, expert, or manufacturing link.
Tomlyn (Vetoquinol USA) discloses NASC membership and two named, credentialed veterinarians, but only on pages outside primary navigation, and publishes no per-active dose panel...
Pawfy is stronger on buyer-facing label access, named experts, and quality-system statements (NASC, cGMP, SQF) than the marketplace norm, but its testing claims and outcome percentages remain unverifiable: no named lab, no COA, and a reused statistics block that does not track the product it appears on.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
What's in it
Six of seven product pages checked disclose a complete active-by-active dose panel with a defined serving size.
Two named DVMs (Dr. Whitney Dettmer and Dr. Daisy May) appear directly on product pages with ingredient-specific commentary.
NASC membership, cGMP, and SQF certification are stated publicly across multiple product pages.
What's not in it
No named third-party laboratory, public COA, or lot-level lookup was found despite a '3rd Party Lab Tested' badge on every checked product page.
The same unsourced outcome-percentage block is reused verbatim across unrelated product categories rather than reflecting product-specific findings.
The manufacturing facility is disclosed only at the country level; no facility name, city, or state was found in any reviewed source.
Pawfy is stronger on buyer-facing label access, named experts, and quality-system statements (NASC, cGMP, SQF) than the marketplace norm, but its testing claims and outcome perc...
Verified transparency record for BIXBI as of 2026-07-03. Twenty-three public pages were fetched and archived across two verification passes, including the brand's Quality Assurance, Pet Safety Assurance, and About pages (which carry most of the brand's testing and formulation-team disclosure) plus a broader marketing-surface review (homepage, category pages, Magazine editorial hub, two representative posts). All eight rubric criteria are scored 'verified' against the tier ladder.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Hip-and-joint jerky treats disclose exact per-active doses (Glucosamine 2,400 mg/kg min, Chondroitin Sulfate 1,200 mg/kg min) on the guaranteed-analysis panel.
Quality Assurance and Pet Safety Assurance pages name specific tested contaminants and pathogens (salmonella, E.coli, listeria, heavy metals, mycotoxins, aflatoxin, ochratoxin) and state batches are held until results are approved.
The mushroom-supplement sub-line is labeled 'NASC Audited Member' in visible page-body copy, alongside disclosed FDA/USDA facility audits and SQF/BRC/IFS or GMP-audited production facilities.
What's not in it
No individual formulator, nutritionist, or veterinarian is named anywhere on the public site; only role/credential descriptions are given.
No third-party testing laboratory is named and no public, buyer-facing lot-level COA lookup is published; the Certificates of Analysis described are supplier-to-BIXBI documents reviewed internally.
All four mushroom-supplement SKUs disclose their active mushroom-species blend only as one combined milligram weight, not per-species amounts.
Verified transparency record for BIXBI as of 2026-07-03. Twenty-three public pages were fetched and archived across two verification passes, including the brand's Quality Assura...
Verified transparency record for Dr. Harvey's. Twelve public sources were fetched and archived on 2026-07-03; every rubric item was checked against the archived HTML, and every exact_quote was confirmed to appear verbatim in its cited source. Absence claims (named experts, facility identity, COA access) were actively probed via the site's XML sitemap and direct URL checks before being confirmed or refuted.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Closed Science
The brand publishes strong testing or COA evidence but does not surface ingredient rationale, named experts, or finished-formula evidence. Testing alone is not enough to make the science verifiable.
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
Manufacturing facility is named at the street, city, and state level (200 Industrial Way West, Eatontown, NJ) with disclosed NASC membership, FDA registration, and cGMP language.
Two named individuals are connected to the brand: formulation lead Dr. Michael Shen and veterinary endorser Dr. Julia Roach, though neither page states a formal credential.
Several product label panels, including Coenzyme Q10 and the Allergy + Immune Soft Chews, disclose full per-active milligram amounts rather than a combined blend total.
What's not in it
The flagship Ortho Flex joint-support supplement discloses its 24 named actives, including Chondroitin Sulfate, as a single 3.3-gram 'proprietary Blend' with no per-active amounts.
No archived page cites a specific study, author, journal, or clinical trial for any ingredient or finished product.
No public lot-linked COA lookup or named third-party testing laboratory was found; direct probes of /pages/coa, /pages/quality, and similar handles returned 404.
Verified transparency record for Dr. Harvey's. Twelve public sources were fetched and archived on 2026-07-03; every rubric item was checked against the archived HTML, and every ...
Animal Essentials names a Veterinary Advisory Board member and discloses FDA-registered, GMP-compliant, NASC-certified manufacturing on its FAQ page, but its dose disclosure and testing-COA transparency are held down by
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Closed Science
The brand publishes strong testing or COA evidence but does not surface ingredient rationale, named experts, or finished-formula evidence. Testing alone is not enough to make the science verifiable.
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
A named individual, Dr. Evelyn Kass Williamson, is identified as a Veterinary Advisory Board member with a defined role, reachable from primary navigation.
The FAQ discloses FDA-registered, GMP-compliant manufacturing and NASC certification, and every checked product page carries a consistent per-ingredient mechanism-level rationale section.
Marketing language stays in support/maintain framing site-wide, with no disease-treatment or unqualified clinical-proof claims found anywhere in the crawled footprint.
What's not in it
Three of five checked supplement SKUs (the entire crawled Veterinarian's Apawthecary sub-line) disclose only a combined-total proprietary blend, not a per-active mg breakdown.
No ingredient-level study, author, or named finished-formula trial was found anywhere on the site.
Testing is claimed brand-wide but no third-party laboratory is named and no public, lot-linked COA is available.
Animal Essentials names a Veterinary Advisory Board member and discloses FDA-registered, GMP-compliant, NASC-certified manufacturing on its FAQ page, but its dose disclosure and...
Garmon Corp. (operating as NaturVet); subsidiary of Swedencare AB
Temecula, California
56.5/100
as of 2026-05-23
Disclosure Gaps
NaturVet is a 30+ year mass-market brand whose substance evidence is unusually disciplined at the label panel (per-active mg disclosure across the line is real) and at the manufacturing identity layer (Temecula, CA facility, FDA / UL / NASC stack). The brand falls into 'Disclosure Gaps' band because it offers no named veterinary expert, no science / mechanism content, and no per-lot COA lookup despite extensive 'veterinarian formulated' marketing. The 70-dog joint-care trial citation is a substantive bright spot but is isolated from any broader citation discipline.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Per-active dose disclosure (mg / IU / mcg / CFU) is consistent across nine sampled PDPs spanning All-In-One, Senior, Calming, Urinary, Hip/Joint, Allergy, Digestion, and Breed-Specific categories — only one proprietary-blend instance found (ArthriSoothe-GOLD's 130 mg enzyme blend with named components).
Manufacturing identity disclosed at city / state level (Temecula, California, in-house facility) with FDA registration, UL third-party facility audit, NASC founding-preferred-supplier seal verified on the NASC registry, and cGMP compliance — facility-level transparency above mass-market median.
Advanced Joint Care PDP cites a real finished-formula 70-dog placebo-controlled trial with a quantified effect size (2.6 greater odds of activity increase at 25 days vs. placebo) and a 'Results may vary' qualifier — substantive citation discipline rare among mass-market competitors, though no publication link is provided.
What's not in it
Zero named veterinarians, formulators, or scientific advisors on the brand surface. The 'veterinarian formulated' framing appears on every PDP, the home page strip, and the A Step Ahead landing page without a single verifiable named individual; on-site search for 'Nardi' (the advisor identified in NaturVet's May 2026 press release) returns no results, and no team / experts / advisory-board page exists.
No Science, Research, Studies, or How-It-Works page exists (probed URLs return 404 or 403). PDP-level ingredient rationale is single-sentence role assertion ('Milk Thistle to help maintain liver health') without mechanism explanation, dose-response discussion, or per-ingredient citation. No PubMed links anywhere in the blog or PDP surfaces.
No public per-lot COA lookup. UL audits the facility but the lab performing per-batch contaminant / microbial / potency assays is not named, and contaminant analytes are not enumerated. NASC's required random product testing is described in plain English but results are not surfaced.
Garmon Corp. (operating as NaturVet); subsidiary of Swedencare AB
NaturVet is a 30+ year mass-market brand whose substance evidence is unusually disciplined at the label panel (per-active mg disclosure across the line is real) and at the manuf...
Rx Vitamins for Pets is a professional-channel supplement brand with real, PDF-based dose and quality-program disclosures once a buyer clicks through from the product page, but its public evidence stops short of the two hardest tests: no named individual stands behind any formula, and no buyer can look up a lab report for a specific bottle. NASC certification and per-active dose panels are the strongest disclosures; testing/COA access and named-expert identity are the largest gaps.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Every sampled product links a downloadable brochure or sell sheet from its PDP with a complete per-active mg/IU/mcg panel and defined serving size.
NASC certification is disclosed on three independent product documents and the full line catalog, and a Technical Report for one product cites roughly 35 dated journal references with author and journal information.
Claims are generally support-oriented rather than direct cure claims on the consumer-facing PDPs.
What's not in it
No public COA lookup, named testing lab, lot-level traceability, or contaminant/microbial panel was found anywhere on the site or in the full 24-page catalog.
No named veterinarian, formulator, or scientific advisor was disclosed on any page checked, including the full product catalog and the one product-level Technical Report.
No manufacturing facility is named at the facility, city, or state level; the Oldsmar, Florida address is a business address, not a disclosed manufacturing site.
Rx Vitamins for Pets is a professional-channel supplement brand with real, PDF-based dose and quality-program disclosures once a buyer clicks through from the product page, but ...
Zesty Paws is a high-distribution, mass-market pet supplement brand with a real, named quality-system baseline (NASC membership with a described independent audit, GMP certification) but an evidence layer that thins quickly past that baseline. Across the eight rubric criteria, the brand's modal pattern is anonymous-collective expert language despite repeated vet-invoking branding, proprietary-blend or undisclosed dose labeling on 4 of 5 sampled flagship products, country-level (not facility-level) manufacturing disclosure, scattered branded-ingredient mechanism mentions that do not generalize catalog-wide, and CBD-only testing transparency for an active line that has moved past CBD SKUs. The Native Canine Probiotic landing is a markedly more disciplined evidence page — honest about its pending RCT — that does not yet generalize to the broader catalog.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Honest qualifier discipline on the Native Canine Probiotic landing — the brand publicly states the full RCT is forthcoming (H1 2026) rather than implying a finished study already exists, and labels small-sample data as preliminary.
NASC Quality Seal membership and GMP certification are both explicitly named and described (not just generic quality language), plus a WCAG 2.2 / ADA accessibility statement with a named tooling partner (TestParty), giving the brand a genuine baseline of structural trust signals even though facility identity itself is disclosed only at the country level.
'Clinically studied' language is correctly attached to specific branded ingredients (Suntheanine on Calming Bites, DE111 on Probiotic Bites, OptiMSM on Mobility) rather than to the finished product, and a direct search of the sampled public surface found no disease-treatment or cure-language claims — a meaningful piece of claim discipline relative to typical category practice.
What's not in it
No named DVM, formulator, scientific advisor, or board member is identified anywhere on the public surface — despite 'Vet-trusted' framing, a 'Vet Strength' product line, and a 'For Veterinary Professionals' nav placement that uses 'developed with scientific and veterinary input' language.
The 'Product Test Results' page in the footer is scoped exclusively to legacy CBD SKUs and returns 'Lot number doesn't exist' for the active catalog; the active 80+ supplement SKUs have no lot-linked COA program, no named third-party laboratory, and no contaminant or microbial panel disclosure.
Per-active dose disclosure is inconsistent across the line: the dog 8-in-1 partially breaks out two actives, Hip & Joint uses a single 1510 mg proprietary blend with no per-active split (and its Chondroitin Sulfate source itself varies by flavor — Bovine vs. Porcine — without being flagged above the fold), Probiotic Bites discloses blend-level CFU only alongside a marketing claim of 'six strains' against a three-strain ingredient panel, and Calming Bites and the Cat 8-in-1 Mousse list ingredients with no doses at all.
Zesty Paws is a high-distribution, mass-market pet supplement brand with a real, named quality-system baseline (NASC membership with a described independent audit, GMP certifica...
Dogzymes has one of the better label-access paths among small supplement brands, especially for probiotics and its multinutrient flagship, with per-active guaranteed analysis on most SKUs reviewed. Its public footprint still lacks named veterinary or formulation experts, third-party lab testing records, a disclosed manufacturing facility, and study citations, and one product in the line uses an undosed proprietary blend.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Most product pages disclose CFU counts, named strains, and per-active guaranteed analysis with no proprietary blend.
Official pages explain probiotic, prebiotic, enzyme, and sourcing rationale, including one specific ingredient-selection example (algal oil vs. fish oil).
The company names its founder and leadership by name with a public origin story, though not as credentialed veterinary or formulation experts.
What's not in it
No named veterinarian, nutritionist, microbiologist, or credentialed formulation reviewer was found — only a named founder with a non-credentialed, experience-based background.
No public COA lookup, named lab, lot-specific report, or manufacturing facility disclosure was found.
One product (Pancreas Support) bundles seven named ingredients into a single undosed proprietary blend line, and evidence pages are reachable only through the footer, not primary navigation.
Dogzymes has one of the better label-access paths among small supplement brands, especially for probiotics and its multinutrient flagship, with per-active guaranteed analysis on...
Rebuilt research record for Pet Wellbeing from the archived 13-surface evidence set (2026-07-03). Every rubric item carries verified evidence, a verbatim quote, gap, and confidence level.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
A genuinely strong expert surface: staff veterinarian Dr. Janice Huntingford (DVM, DACVSMR, CVA, CVPP, CTCVMP) with a named clinic, plus a second credentialed vet, on a primary-nav page.
Per-herb rationale on product pages and a candid FAQ: organic claims declined where unverifiable, the proprietary flavor blend disclosed as such, USA GMP manufacture and three-tier sourcing stated.
Tinctures disclose full botanical identity with Latin names and total mg-per-ml concentration.
What's not in it
A dedicated oncology-support page markets Life Gold 'especially for dogs with cancer' with an unpublished compatible-with-treatments safety claim.
'Shown in animal studies' and 'tested by our holistic veterinarians' appear with no study, protocol, or citation anywhere; the site library contains no references.
No named laboratory, COA, lot lookup, or panel results exist; per-herb amounts within blends are not published.
Rebuilt research record for Pet Wellbeing from the archived 13-surface evidence set (2026-07-03). Every rubric item carries verified evidence, a verbatim quote, gap, and confide...
PetNC discloses more on manufacturing and label-dose than its initial review credited — the brand names its facility's city and state with GMP and NASC status, and its own product pages show complete per-active dosing across every SKU tested in this pass. Evidence citations and named experts remain the brand's clearest gaps: no clinical studies, named laboratory, or named veterinary reviewer were found anywhere in the public record after an active search.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
The brand's own product pages disclose a complete active-by-active milligram panel, confirmed consistent across four different product categories.
The official PetNC page and three independent corroborating sources name the manufacturing facility's city and state (Tempe, AZ) along with GMP compliance and NASC Quality Seal status.
Marketing language stays within joint-support and quality-of-life framing without disease-treatment claims or unqualified clinical-certainty language.
What's not in it
No named veterinarian, nutritionist, or product reviewer was found after an active search across 13 public sources.
No public COA, named third-party laboratory, or lot-specific report was found; an 18-URL direct probe for a testing or quality-assurance page returned 404 in every case.
The brand does not cite any clinical studies or distinguish ingredient-level research from finished-formula evidence anywhere in the reviewed public sources.
PetNC discloses more on manufacturing and label-dose than its initial review credited — the brand names its facility's city and state with GMP and NASC status, and its own produ...
Verified transparency record for Grizzly Pet Products following a hostile adversarial verification pass on 2026-07-03. All 14 archived sources were re-fetched, all 8 exact quotes confirmed verbatim, and every criterion re-scored against the tier-ladder anchors. The brand's label and manufacturing-quality-system disclosures verified stronger than the original preliminary pass found, while testing/COA and named-expert disclosure verified weaker — both scored against directly probed evidence rather than assumed from generic marketing language.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Closed Science
The brand publishes strong testing or COA evidence but does not surface ingredient rationale, named experts, or finished-formula evidence. Testing alone is not enough to make the science verifiable.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Every one of the 7 live product pages discloses a complete per-active mg/mcg or Guaranteed Analysis panel with a full inactive-ingredients list and zero proprietary-blend language found anywhere on the site.
A dedicated, primary-navigation science page explains the biological mechanism and bioavailability differences between Omega-3, -6, and -9 fatty acids, with one externally cited source for a sourcing claim.
NASC membership and region-level (Alaska) sourcing detail are disclosed on primary pages, though without a named facility address.
What's not in it
No public testing program, named laboratory, contaminant/microbial/potency panel, or COA lookup exists anywhere on the site.
No named veterinarian, nutritionist, formulator, or scientific advisor is disclosed; the closest signal is an unnamed 'Founded by a scientist' claim.
The one genuine external citation found on the site supports an environmental-sourcing claim, not a health or efficacy claim, and no finished-formula clinical evidence is disclosed for any product.
Verified transparency record for Grizzly Pet Products following a hostile adversarial verification pass on 2026-07-03. All 14 archived sources were re-fetched, all 8 exact quote...
Pet Naturals publishes per-active dose panels on every PDP reviewed, including low-priced problem-solver SKUs, and discloses Vermont manufacture under SQF, cGMP, and NASC founding-member standards. Claim language stays in the support/help register with qualifier discipline. The disclosure gaps cluster around people and proof: no named expert appears anywhere on the brand surface, no laboratory is named, no COA is accessible, and no study citation supports the ingredient glossary's one-line role descriptions.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Per-active dose disclosure holds across all twelve PDPs reviewed — from flagship Calming (Thiamine 35 mg, Colostrum Calming Complex® 5 mg, L-Theanine 5 mg) to the $10.50 Breath Bites with its 'Spirulina 100 mg yielding Chlorophyll 2 mg' yield spec — with complete inactive lists and per-weight dosing on every page.
Manufacturing and quality-system disclosure is concrete for the mass-market tier: Vermont manufacture, SQF-certified facilities, cGMP adherence, and NASC founding-member status (via parent FoodScience, LLC) with the seal program's five quality-control requirements enumerated on a dedicated page.
Claim register is consistently restrained — support/help language with 'occasional' qualifiers, zero 'clinically proven' or disease-treatment language found, and a published review-moderation policy removing reviews that imply disease claims.
What's not in it
No named veterinarian, nutritionist, or formulator appears anywhere on the brand surface — About Us names no people, the blog is house-bylined, and no team or experts page exists.
Testing is asserted (third-party ingredient testing, NASC random independent-lab testing) but no laboratory is named, no COA is viewable or requestable on-site, and nothing connects testing to specific lots or enumerates panel analytes.
The flagship calming active is a 5 mg proprietary 'Colostrum Calming Complex® Biopeptide Blend' described only as 'bioactive proteins,' probiotic SKUs stop at genus/species without strain designations, and manufacturing identity is held at state level rather than facility, city, and state.
Pet Naturals publishes per-active dose panels on every PDP reviewed, including low-priced problem-solver SKUs, and discloses Vermont manufacture under SQF, cGMP, and NASC foundi...
Verified transparency record for kin+kind following a hostile adversarial pass completed 2026-07-03. All 15 sources were fetched and archived; every rubric criterion's exact_quote was checked verbatim against the archived HTML, with 2 of 8 quotes replaced after the originals were found to be non-evidentiary UI-chrome text. Every absence claim (named veterinarian, facility-level quality certification, COA lookup) was actively probed via sitemap enumeration and direct URL testing before being confirmed. All 8 criteria are marked verified with score_status locked and anchor language cited in the evidence text.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Closed Science
The brand publishes strong testing or COA evidence but does not surface ingredient rationale, named experts, or finished-formula evidence. Testing alone is not enough to make the science verifiable.
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
The Flea+Tick spray line publishes a full active-ingredient percentage panel directly on the product page (e.g., Peppermint Oil 1.00%, Rosemary Oil 1.00%, Cedarwood Oil 0.20%).
A real facility location (New Jersey) is disclosed for its US manufacturing, and the Hip+Joint supplement's curcumin-bioavailability claims link two live, publicly-accessible NCBI/PubMed articles as ingredient-level research.
Evidence pages for ingredients, manufacturing, and the vet-formulated claim are reachable in one click from a primary-header dropdown menu on every page of the site.
What's not in it
The veterinarian behind the brand's repeated 'vet formulated' and 'designed by our own veterinarian' claims is never named or credentialed anywhere in the site's public footprint, including on a page built specifically around that claim.
No third-party testing laboratory, certificate-of-analysis lookup, or contaminant/microbial/potency panel is disclosed anywhere on the site; direct probes of common transparency-page handles (COA, lab-results, quality-assurance, testing) all returned HTTP 404.
The Flea+Tick line's above-the-fold 'CLINICALLY PROVEN FLEA & TICK REPELLENCY... Tested to deliver over 90% efficacy' claim has no visible study, author, or citation anywhere it appears, despite the brand showing real citation discipline for its supplement line.
Verified transparency record for kin+kind following a hostile adversarial pass completed 2026-07-03. All 15 sources were fetched and archived; every rubric criterion's exact_quo...
Hostile-verified research record for Wholistic Pet Organics from 14 independently live-fetched surfaces (2026-07-03): home, About, FAQ, and 11 product/support pages spanning the brand's roughly 27-SKU catalog. Every rubric item carries verified evidence, a verbatim re-confirmed quote, gap, and confidence level. An adjudication re-check on 2026-07-03 corrected two scores (testing-coa-transparency, manufacturing-quality-system-transparency) after already-archived evidence of NASC membership and an FDA-registered facility, missed by the first pass, was surfaced, verified against the source byte-for-byte, and independently corroborated on NASC's own member directory.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Evidence Buried
The brand technically publishes meaningful science, evidence, testing, or expert disclosure, but buyers cannot reach it without dedicated effort. Evidence that exists but is hard to find counts less.
What's in it
Genuine per-active mg/potency-unit disclosure with mechanism text exists on several SKUs (Joint Mobility, Run Free, Digest All Plus), not just an ingredient-identity list.
NASC (National Animal Supplement Council) membership and a passed facility audit, externally corroborated on NASC's own member directory, plus a self-disclosed FDA-registered New Hampshire manufacturing facility.
Unusual honesty about what the brand is not: 'We are not veterinarians and do not, in any way, mean to diagnose or treat,' paired with a humble claim register offering choices rather than cures.
What's not in it
The brand's own flagship (Canine Complete) and its direct cat-line counterpart (Feline Complete) publish zero per-active amounts, even though other SKUs in the same catalog do.
The claimed five-science 'backgrounds' are attached to no named person beyond a family surname, and no outside expert, advisor, or reviewer is named anywhere.
The NASC facility audit is a manufacturing/practices audit, not a per-batch laboratory program — no named testing lab, COA, lot traceability, or contaminant/microbial/potency panel exists anywhere, and facility identity stops at the state level (no city or facility name); 'superior' claims appear on two independent pages with nothing published to support them.
Hostile-verified research record for Wholistic Pet Organics from 14 independently live-fetched surfaces (2026-07-03): home, About, FAQ, and 11 product/support pages spanning the...
Compana Pet Brands LLC (the site's own UGC Policy separately identifies the operating entity as "Vet's Best, LLC d/b/a Compana Pet Brands" — the two legal pages use different primary-entity framing; both name the same parent).
707 Spirit 40 Park Drive, Suite 150, Chesterfield, MO 63005, United States (Compana Pet Brands LLC corporate/privacy-contact address; not disclosed as a manufacturing facility).
52.5/100
as of 2026-07-03
Disclosure Gaps
Rebuilt and adversarially verified research record for Vet's Best from sixteen live-fetched surfaces (2026-07-03): homepage, About, FAQs, Education, Contact, Privacy Policy, UGC Policy, satisfaction-guarantee policy, and seven product pages. Every rubric item carries verified evidence, a verbatim quote checked against archived raw HTML, gap, and confidence level; absence claims were actively probed against the brand's own sitemap rather than assumed.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
What's in it
Complete per-active panels on 4 of 7 checked supplement SKUs (Hip & Joint, Healthy Coat, Seasonal Allergy, Urinary Tract Support), with full inactive lists and weight-banded directions.
A named veterinary founder (Dr. Dawn Curie Thomas, DVM, 1989) and unusually honest FAQ cautions, including not-intended-to-cure framing and interaction warnings.
NASC Quality Seal disclosed on two product surfaces (Gentle Dental powder via the FAQ, Healthy Coat Tablets on its own product page) with an accurate description of program requirements.
What's not in it
The About page claims ingredients are 'scientifically proven to be safe and effective' with no citation anywhere on the site.
No third-party laboratory, COA, lot lookup, or test panel exists on any fetched surface.
No current veterinarian or reviewer is named behind the pervasive 'veterinarian-formulated' claim (confirmed on all 7 checked product pages), and no manufacturing facility or cGMP disclosure exists.
Compana Pet Brands LLC (the site's own UGC Policy separately identifies the operating entity as "Vet's Best, LLC d/b/a Compana Pet Brands" — the two legal pages use different primary-entity framing; both name the same parent).
Rebuilt and adversarially verified research record for Vet's Best from sixteen live-fetched surfaces (2026-07-03): homepage, About, FAQs, Education, Contact, Privacy Policy, UGC...
Native Pet is a recognizable DTC dog supplement brand with one substance-positive expert disclosure (Dr. Dan Su, board-certified veterinary nutritionist named on the home page and PDPs) and one substance-positive testing signal (Clean Label Project certification on The Daily). The brand falls into the Disclosure Gaps band because per-active doses are image-only or absent, two products use proprietary blends, marketing uses clinical-style language without underlying citations, there is no dedicated team or testing page, and manufacturing is disclosed at country level only.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Evidence Buried
The brand technically publishes meaningful science, evidence, testing, or expert disclosure, but buyers cannot reach it without dedicated effort. Evidence that exists but is hard to find counts less.
What's in it
Names Dr. Dan Su, MS, DVM, DACVIM (Nutrition) on the home page and on product PDPs as formulator — DACVIM (Nutrition) is a real board-certified veterinary specialty credential.
Clean Label Project certification on The Daily flagship is a substantive third-party signal with a defined 150+ contaminant panel — including heavy metals, pesticides, and plastics.
Long-form blog includes ingredient-level honesty and citation (the Glucosamine blog explicitly acknowledges thin veterinary evidence for the ingredient and links 10 PubMed/NCBI sources), and the Philosophy page articulates a six-point formulation pact with concrete commitments (max 5 inactive ingredients, no fillers, in-house formulation).
What's not in it
No dedicated team, testing, science, or trust-hub pages on the brand surface — Dr. Dan Su has no public bio page and no documented scope/employment relationship; testing disclosure is concentrated on a single product; mechanism content is buried in blog.
Proprietary probiotic blends on Senior Daily and Skin+Coat Chews, and no per-active mg/IU/mcg disclosure in inline PDP text across any product reviewed — supplement facts panels render only inside product images, which fails buyer-verifiability for screen readers, comparison shopping, and accessibility.
Marketing language uses 'clinically researched,' 'clinically studied,' 'research-backed,' 'science-backed,' and 'It's been proven to' framing across the home page, flagship PDP, retail page, and colostrum blog without surfacing any citation nearby; the one page that does cite real PubMed sources (the Glucosamine blog) is not linked from primary navigation and its citations do not substantiate the flagship's own point-of-sale claims; no finished-formula clinical trial exists on any Native Pet product.
Native Pet is a recognizable DTC dog supplement brand with one substance-positive expert disclosure (Dr. Dan Su, board-certified veterinary nutritionist named on the home page a...
Solid Gold is strongest where its flagship SeaMeal supplements are concerned: buyers can verify quantified dosing, NASC membership, and country-level manufacturing with a named parent company. That strength does not extend evenly across the rest of the supplement line, where checked SKUs show no quantified dosing, and named experts, public lab reports, and facility-level manufacturing detail remain unconfirmed anywhere in the brand's public footprint.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
SeaMeal powder and chews both publish a complete guaranteed analysis with quantified omega and digestive-enzyme values, independently corroborated on a retailer listing.
NASC Primary Supplier status is publicly confirmed, and manufacturing location is disclosed at the country level (USA and Thailand) alongside a named parent company (H&H Group) and B Corp claim.
Marketing language avoids disease-treatment or guaranteed-outcome claims, and the brand proactively and transparently addresses the FDA DCM investigation rather than staying silent on it.
What's not in it
No named veterinarian, nutritionist, or formulator was found anywhere on the reviewed pages -- only anonymous 'vet survey' and 'team of scientists' language.
Per-active dosing is confirmed on SeaMeal but absent on other checked supplement SKUs (Mobility Chews, Multivitamin Chews), and no public COA, named lab, or lot-level testing report was found.
Recurring unqualified 'transformational' outcome language appears in the brand's own meta description and its Amazon manufacturer content without a supporting citation.
Solid Gold is strongest where its flagship SeaMeal supplements are concerned: buyers can verify quantified dosing, NASC membership, and country-level manufacturing with a named ...
The Honest Kitchen's most substantive evidence -- a cGMP/21 CFR 117 sourcing citation and a named veterinarian testimonial -- lives on pages (Why Human Grade, Vet Resources) reachable only through an embedded promotional panel or sitemap discovery, not primary site navigation. Its supplement-specific evidence is weaker still: Perfect Form and comparable SKUs group or omit per-active amounts, no clinical study is cited for the supplement line, and the brand's actual formulators remain unnamed even where a testimonial from a named outside veterinarian is surfaced.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
What's in it
Perfect Form names active ingredients per one teaspoon and states there are no inactive ingredients.
The Why Human Grade page cites current good manufacturing practices and 21 CFR 117 for its human-food-facility standard, and discloses a supplier-level Certificate of Analysis requirement for incoming ingredients.
The Vet Resources page names one veterinarian, Dr. Leilani Alvarez, DVM, DACVSMR, with a quoted endorsement, and references an independent ISO accredited laboratory used for recipe nutrient testing.
What's not in it
No public COA lookup or named third-party laboratory was found for Perfect Form or any other supplement/broth batch.
The formulation team behind The Honest Kitchen's recipes ('leading veterinarians... nutritionists and PhD food scientists') is never named; the one named veterinarian gives a customer-style testimonial, not a formulation or advisory role.
Perfect Form and two other supplement-line SKUs checked do not disclose individual active amounts, and none has a clinical citation tied to the finished product.
The Honest Kitchen's most substantive evidence -- a cGMP/21 CFR 117 sourcing citation and a named veterinarian testimonial -- lives on pages (Why Human Grade, Vet Resources) rea...
Vetoquinol USA's strongest disclosure is structural: an audited NASC membership with cGMP manufacturing and, on the Flexadin joint chews, active milligram amounts plus a cited ingredient study. Disclosure thins across the rest of the supplement line, where Triglyceride OMEGA and Zylkene report blend totals or capsule strengths rather than active-by-active amounts, the Zylkene 'clinically proven' claim shows no on-page citation, no veterinarian or formulator is named, and there is no public COA lookup or named testing laboratory.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Audited NASC membership with an explicit cGMP statement and NAERS adverse-event participation, placing structural quality-system disclosure above the category median.
The Flexadin Advanced chews publish active collagen amounts in milligrams with defined serving sizes and complete inactive-ingredient lists.
The Flexadin pages cite an attributed, dated study (D'Altilio et al, 2007) and mark their headline comparative claim with a qualifying asterisk.
What's not in it
Label disclosure varies across the line: Triglyceride OMEGA reports fish-oil blend totals without per-active EPA/DHA amounts and Zylkene gives capsule strengths without isolating the alpha-casozepine amount.
No veterinarian, nutritionist, or formulator is named anywhere on the site; expertise is conveyed only through 'veterinarian recommended' and vet-channel framing.
No public certificate-of-analysis lookup, named testing laboratory, or contaminant/microbial/potency panel is published, and manufacturing facilities are not named at facility, city, and state level.
Vetoquinol USA's strongest disclosure is structural: an audited NASC membership with cGMP manufacturing and, on the Flexadin joint chews, active milligram amounts plus a cited i...
Verified transparency record for Ark Naturals, current as of the 2026-07-03 research pass. All 8 rubric criteria were re-scored against verbatim quotes from freshly archived source pages, including a sitemap-based check for pages the brand does not link from its own navigation.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Two secondary supplement SKUs (Joint Rescue, Happy Traveler) disclose complete active-by-active mg amounts with weight-tiered feeding directions.
A dedicated science article, reachable from primary navigation, explains the dental line's antioxidant ingredient with two verifiable PubMed citations and an explicit disease-claim disclaimer.
Country-level manufacturing disclosure ('Made in USA,' NASC-approved on two SKUs) is present, though not extended to facility identity or full-line testing coverage.
What's not in it
The flagship 'clinically proven' Protection+ line names its active ingredient (Astaxanthin) without disclosing an amount, and its specific plaque/tartar percentage claims link to a dead citation on both pages that reference one.
No named veterinarian, formulator, or scientific advisor was found anywhere across 16 pages fetched in this pass.
No named testing laboratory, public COA, or contaminant/microbial/potency panel was found anywhere; NASC-approved language covers only 2 of 15 catalog SKUs.
Verified transparency record for Ark Naturals, current as of the 2026-07-03 research pass. All 8 rubric criteria were re-scored against verbatim quotes from freshly archived sou...
Purina Pro Plan Veterinary Supplements discloses per-active doses well across most of its line — full mg panels on soft chews, per-strain CFU on probiotic powders — and keeps its own marketing comparatively measured. The brand-direct site is built for purchasing rather than verification: it names the NASC Seal on two SKUs and U.S. company-owned manufacturing in aggregate, but publishes no named experts, no study citations behind its efficacy claims, and no product testing or lot-linked COA. Substance gaps cluster on citation, expert identity, and testing rather than on labels.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Soft-chew SKUs disclose full per-active milligram panels (Joint Care and Skin Care itemize every active with exact mg) and the probiotic powders publish per-strain CFU with defined serving sizes — strong, format-appropriate label disclosure across most of the line.
Marketing on the brand's own pages is generally measured, using hedged verbs, six-week onset qualifiers, and a comparator-baseline hydration claim, and it omits the aggressive efficacy statistics that appear in third-party retail copy.
The Skin Care and Multi Care pages name the NASC Quality Seal (Certified by the National Animal Supplement Council), and the 'Our Difference' page discloses U.S. company-owned manufacturing with an aggregate daily quality-check figure.
What's not in it
No veterinarian, nutritionist, or formulator is named anywhere on the brand-direct site; expert involvement is presented only as an anonymous 'collaboration among Purina nutritionists, researchers and veterinarians.'
Efficacy language such as 'proven to promote intestinal health' and 'shown to help dogs maintain calm behavior' is not paired with accessible study citations, and the pages do not distinguish strain-level research from finished-formula evidence.
There is no public COA lookup, no named third-party laboratory, and no disclosed contaminant/microbial/potency panel; the 311-URL sitemap contains no science, testing, or named-expert page.
Purina Pro Plan Veterinary Supplements discloses per-active doses well across most of its line — full mg panels on soft chews, per-strain CFU on probiotic powders — and keeps it...
Rebuilt research record from Internet Archive snapshots (About Us 2025-11-18; Veterinary Supplements 2025-11-26) because the live site refuses automated access. Every rubric item carries verified evidence, a verbatim quote, gap, and confidence level.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Address-level facility disclosure — 1200 W. Royal Lee Drive, Palmyra, WI — with an owned-farm, farming-through-shipping quality chain and USDA-accredited organic certification.
Real species-physiology formulation rationale on the public page (omnivore canine vs obligate-carnivore feline vs equine phytonutrient logic).
Named continuity: founder Dr. Royal Lee and the owning DuBois family, across 90-plus years.
What's not in it
Clinical evidence, product documentation, and panels route behind practitioner accounts — the public buyer surface shows philosophy, not documents.
No current named veterinarian or formulator for the Veterinary Formulas line on public surfaces.
A bare 'Safe and effective' assertion on the equine line, and no public COA, named lab, or lot access.
Rebuilt research record from Internet Archive snapshots (About Us 2025-11-18; Veterinary Supplements 2025-11-26) because the live site refuses automated access. Every rubric ite...
STRELLALAB discloses more on individual official product pages than a marketplace-only review would suggest -- including per-active mg amounts on two SKUs -- but that disclosure is scattered and incomplete across the line, and the brand does not publish named experts, lab testing, or clinical citations anywhere in its reachable public footprint. Its NASC quality-system membership, while real, is not accessible from the brand's own website.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Official product pages disclose per-active milligram amounts for some ingredients on the flagship glucosamine and omega chews.
A named quality-system membership (NASC Primary Supplier) and consistent Made-in-USA manufacturing language are both publicly confirmed.
Official pages show company contact information, a full company address, and clear supplement categories.
What's not in it
No named veterinarian, nutritionist, or formula reviewer was found; 'Vet-Approved' language appears without any named individual.
No public COA lookup, named laboratory, or lot-level test report was found, and the brand's own NASC membership signal is not linked anywhere on its own website.
Per-active dose disclosure is inconsistent across the line -- absent on the probiotics SKU and missing the glucosamine product's own namesake Chondroitin active.
STRELLALAB discloses more on individual official product pages than a marketplace-only review would suggest -- including per-active mg amounts on two SKUs -- but that disclosure...
Dinovite publishes consistent guaranteed-analysis panels and full ingredient lists across its line, with exact omega doses available in its FAQ and per-active milligrams on the dental sub-line. Disclosure stops at the label: the brand names no laboratory, publishes no COAs, discloses no quality system beyond made-in-USA badges, and its dental line's clinical claims cite no readable studies. One named R&D nutritionist appears on the dental PDPs; the core line's experts remain unnamed.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Every product in the line publishes a complete ingredient list and a guaranteed-analysis panel with quantified minimums — zinc 2 mg/gm, vitamin E 12 IU/gm, taurine 10 mg/gm on the cat formula, total microorganisms 1.0x10^8 CFU/gm — plus stated scoop weights, applied consistently from flagship to puppy SKU.
The dental sub-line reaches the brand's strongest disclosure tier: per-active milligrams (250 mg Canine Oral Health Postbiotic per chew; 253-284 mg per powder scoop) and a named formulator, Dr. Inke Paetau-Robinson, Senior Nutritionist, R&D, quoted on both PDPs.
The FAQ volunteers buyer-protective specifics that are rare for legacy direct-response brands: exact DHA/EPA doses per teaspoon for both oils, a kelp-thyroid caution, and an explicit statement that the dental clinical studies were conducted with the postbiotic ingredient.
What's not in it
No public testing disclosure exists at any level — no named laboratory, no COA access, no lot traceability, and no testing or quality page; probed URLs return 404 and brand copy contains no third-party-testing language.
No quality-system disclosure — manufacturing is held at made-in-USA badge level plus an unnamed 52,000-square-foot facility reference, with no cGMP, NASC, FDA-registration, or facility identity published.
The dental line's 'clinically proven' and '3 clinical trials' claims, and the flagship's comparative statistics ('83% say Dinovite works better'), are published without any citation, methodology, or readable study.
Dinovite publishes consistent guaranteed-analysis panels and full ingredient lists across its line, with exact omega doses available in its FAQ and per-active milligrams on the ...
Every brand was scored against the same eight buyer-facing questions — doses, ingredient rationale, clinical evidence, named experts, testing & COAs, manufacturing, claim discipline, and findability. Only public, buyer-verifiable evidence was counted. Information available only via support email, retailer-only listings, or unsupported third-party language was not counted.
Brands cannot win on testing alone. A clean COA program does not substitute for ingredient rationale, named experts, or honest finished-formula evidence. Brands that lead on testing alone are flagged with the Closed Science watchout.
How La Petite Labs is scored.
La Petite Labs publishes this report and sells products in this category. Our score is shown above the rankings as a Publisher Benchmark, excluded from the ranking table and from awards. LPL's own gaps (partial COA rollout, no published finished-formula trial yet, no named per-formula scientific owner, manufacturing identity at country level only) are documented under the same evidence rules every other brand is held to.
Annual major review. Quarterly correction windows.
This report is reviewed annually with limited correction windows for material brand updates. Originally published May 22, 2026; evidence reviewed through Jul 3, 2026; rubric v2026.2 applied Jul 3, 2026; report updated Jul 3, 2026. Next scheduled full review: Q2 2027.
v 2026.2 · annual major-update cycle
Brand Correction Policy
Bring documented public evidence. We'll review.
Scores reflect the brand's public surface at the time of review. If a brand has materially updated label disclosure, science pages, named people, testing program, manufacturing facility, COA lookup, or claim-discipline language, it may submit those updates for correction-window review. Updates must be on public brand pages — private materials, correspondence, and retailer-only language are not counted.
Archival Snapshot Policy
Every quoted claim is captured at review time.
Every brand-rubric criterion cites at least one dated, public evidence source with a verbatim quote captured at the time of review; archived page snapshots are being attached to each source as backfill completes. Brands may update their public surface; the score reflects the capture date. Correction requests trigger fresh capture against the current public surface.
View the Evidence Dataset
The complete brand-transparency scoring run, as machine-readable JSON.
The public dataset includes the scoring rubric, criterion definitions, brand-level evidence, source quotes, named experts, testing programs, manufacturing programs, and reasoning used for this report. Published for public review.
La Petite Labs Editorial. Pet Supplement Brand Transparency Report 2026, v2026.2. Originally published May 22, 2026; evidence reviewed through Jul 3, 2026; rubric applied and report updated Jul 3, 2026. https://lapetitelabs.com/pages/pet-supplement-brand-transparency-report
Journalists, researchers, and AI tools are welcome to cite this report and the public dataset with attribution. Scores are version-stamped (v2026.2); each annual edition is archived. Brands may dispute a score through the correction policy above. Methodology: Pet Supplement Brand Transparency Rubric.
It is the flagship trust badge in this report. A brand earns it when it publishes buyer-verifiable evidence across the main pillars — label disclosure, ingredient rationale, clinical evidence, named experts — at a level a buyer can independently check before purchase. The gate is deterministic and the same rule applies to every brand.
What is a Publisher Benchmark?
La Petite Labs publishes this report and sells products in this category. We show our score separately as a Publisher Benchmark, excluded from the ranking table and competitive awards. The same rubric is used, and our own gaps are listed for readers to inspect.
How were the brands selected?
The survey targets the pet supplement brands US buyers most often search for and encounter — large mass-market and veterinary-channel brands, the major direct-to-consumer brands, and category-relevant premium brands — plus the publisher, graded separately. Selection favors market presence, not closeness to any La Petite Labs product line. Each dossier records the brand's selection rationale, and brands are added at each annual review cycle. A brand that believes it belongs in the survey can request inclusion through the correction policy.
How are watchouts decided?
Watchouts surface honest limitations in a brand's public evidence. Scores are deterministic — the same weighted formula applies to every brand. Watchouts are applied through editorial review against fixed public definitions: Closed Science is flagged when testing is strong but ingredient rationale and named experts are weak; Borrowed Evidence is flagged when a brand uses "clinically tested" language without a finished-formula study; Unnamed Experts is flagged when a brand says "vet-formulated" without naming the vet.
Can a brand request a correction?
Yes. Scores reflect the brand's public surface at the time of review. If a brand has materially updated label disclosure, science pages, named people, testing program, manufacturing facility, COA lookup, or claim-discipline language, it may submit those updates for correction-window review. Updates must be on public brand pages — private materials, correspondence, and retailer-only language are not counted.
Higher scores reward
Breadth, disclosure, and substantiation.
Coverage of multiple longevity pathways under one daily formula.
Per-active milligram amounts disclosed on the public label.
Named third-party lab, published Certificate of Analysis, lot-level traceability.
Public substantiation for marketing claims — citations, not adjectives.
Lower scores may mean
Narrower scope, or less of the work published.
The product targets a single problem rather than longevity-system coverage.
Actives are listed without per-serving amounts (proprietary blends).
Testing language is vague — no named lab, no public COA, no lot linkage.
Claims outrun the public evidence record at time of review.
A lower score does not automatically mean a product is unsuitable. It may simply
be narrower in scope, less transparent, or supported by fewer public quality
signals than this rubric rewards.
50
Rank
45.5/100
as of 2026-07-03
Sparse Public Evidence
50
Rank
Wonder Paws
45.5/100
as of 2026-07-03
Sparse Public Evidence
An Amazon-native brand with a real program-level quality stack — NASC primary supplier, completed audit, GMP, FDA-registered USA facility — alongside three sitemap-only advertorial pages that name a real veterinarian wit
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
Line Inconsistency
Disclosure varies materially across the brand line — one product is well-disclosed, others are not. Buyers may not know which product they are comparing.
What's in it
A coherent program-level quality stack on a dedicated NASC page: primary-supplier status, completed NASC audit, GMP adherence, FDA-registered USA production — three named quality-system elements together, not just one.
Real per-active dose figures recur across multiple SKUs and a retailer listing (200 mg prebiotic fiber, 75 mg EPA / 85 mg DHA, 600 mg liquid collagen), even though no SKU publishes a complete panel.
The brand's primary navigable pages (home, NASC, FAQ, flagship product) keep a clean, support-framed claim register with no disease-treatment language or unattributed clinical-proof stamps.
What's not in it
Three sitemap-only, unlinked advertorial pages name a real DVM ('Dr. Paula Simons') under a credential her own institution's faculty page does not document, credit her with co-designing the flagship product, and attribute a specific research finding to her with no citation behind it.
The same advertorial pages misattribute a real 2018 human-skin study (published in Nutrients) to dogs and to a different journal name, plus cite an unattributed conference study and unattributed 'independent laboratory analyses' — none of it reachable from the site's navigation, none of it citable by a buyer.
No product testing artifact anywhere on 15 pages checked: no lab, COA, panel, or lot trace behind the NASC-audit program statement, and no complete per-active panel on any SKU reviewed.
An Amazon-native brand with a real program-level quality stack — NASC primary supplier, completed audit, GMP, FDA-registered USA facility — alongside three sitemap-only advertor...
Adversarially verified record for NUPRO Supplements, refetched and re-anchored on 2026-07-03. All 8 rubric criteria are flagged verified, each with a directly quoted, source-archived verbatim passage from the brand's real site (not the Shopify-pattern URLs the original research pass had guessed) and an explicit tier-anchor justification.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreePublic COA LookupPer-Lot TraceabilityNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
The brand-wide Ingredients page gives every active ingredient a mechanism-level rationale, not just a benefit claim, consistently across the Dog, Cat, and Ferret lines.
NASC (National Animal Supplement Council) membership is publicly, specifically claimed with a description of the independent facility-audit requirement behind the Quality Seal, and is one click from every page's footer.
Marketing language avoids disease-treatment, cure, or guaranteed-results claims across all 24 real pages checked, and the FAQ page includes genuinely disciplined dosing-caution and potency-decay language.
What's not in it
The flagship Original Gold formula — the brand's modal, most-purchased line — discloses zero per-active mg/IU amounts anywhere, even though two secondary lines (Joint & Immunity, Electrolytes) do publish full dosing.
No third-party laboratory, contaminant/microbial/potency panel, or COA lookup exists anywhere on the real site; the only batch-level signal is a printed lot code and expiration date.
No named veterinarian, nutritionist, or formulator appears anywhere on the site; the recurring 'researched and developed by a doctor of nutrition' and 'developed by veterinarians' claims name no individual, credential, or institution.
Adversarially verified record for NUPRO Supplements, refetched and re-anchored on 2026-07-03. All 8 rubric criteria are flagged verified, each with a directly quoted, source-arc...
Amazing Nutritionals is more accessible and more quantitatively labeled than a first pass suggested — most SKUs disclose per-active mg amounts and the brand names a state-level GMP facility reachable from the home-page footer. But its own marketing copy names specific diagnosable conditions as claim targets across most of the line without any clinical citation, and no named expert or public lab report was found anywhere on the site.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Turmeric, cranberry, and omega-3 product pages disclose per-active mg amounts for every named ingredient, with no proprietary blend on those three SKUs.
The brand names a GMP and Organic-Certified manufacturing facility at the state level (Florida) and describes a batch-level testing process, both reachable within one click from the home-page footer.
Testing and manufacturing evidence is publicly footer-linked (FAQ, Why Buy) rather than requiring a support request.
What's not in it
No named veterinarian, nutritionist, or formulator was found anywhere on the site; a repeated 'veterinary science approved' phrase names no individual.
No third-party laboratory, public certificate of analysis, or lot-level lookup was found for any product.
Marketing language names diagnosable conditions (rheumatoid arthritis, staph infection, urinary tract infection) as prevent/eliminate/remedy targets across most of the product line, paired with an unqualified 'Guaranteed results, or your money back!' claim.
Amazing Nutritionals is more accessible and more quantitatively labeled than a first pass suggested — most SKUs disclose per-active mg amounts and the brand names a state-level ...
Research record for Under the Weather from ten live-fetched surfaces, rebuilt 2026-07-03 and re-verified 2026-07-03: home, about, FAQ, reviews, shelters, stores, and four product pages spanning cat and dog calming chews, the Ready Cal gel, and the flagship bland-diet food. Every rubric item carries verified evidence, a verbatim quote, gap, and confidence level; two scores were corrected against tier anchors during the verify pass.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Real per-active panels on both calming-chew SKUs (cat: thiamine 65 mg, L-tryptophan 10 mg, L-theanine 8.5 mg; dog: ginger 60 mg, chamomile 50 mg, L-theanine 20 mg, L-tryptophan 20 mg per serving).
Specific sourcing disclosure: 100% USA human-grade meats — cage-free poultry, grass-fed beef, wild line-caught salmon — plus a repeated, consistent Vermont manufacturing location across five live pages.
Honest vet-routing habits in the FAQ, including a candid "we are not veterinarians" and pregnancy/nursing cautions.
What's not in it
The FAQ claims the products 'have no harmful side effects' — an absolute safety claim no supplement can carry.
The hero's 'Calms in ~30 min' onset claim has no published basis, and the Ready Cal product page names three veterinary journals with no author, year, or link attached to any of them.
No testing artifacts (lab, COA, lot, panel), no named veterinarian behind the vet-formulated claim, and no facility-name, city, or quality-system certification beyond the state-level Vermont disclosure.
Research record for Under the Weather from ten live-fetched surfaces, rebuilt 2026-07-03 and re-verified 2026-07-03: home, about, FAQ, reviews, shelters, stores, and four produc...
Silver Star Brands, Inc., doing business as Native Remedies
Oshkosh, WI, U.S.A.
37.5/100
as of 2026-07-03
Sparse Public Evidence
Rebuilt research record for PetAlive from six live-fetched surfaces (2026-07-03): the hub, FAQ, Ask Our Experts, product finder, a flagship product page (Kidney Support, SKU 351872), and the ailment index. Every rubric item carries verified evidence, a verbatim quote, gap, and confidence level.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Unnamed Experts
The brand uses "veterinarian formulated," "expert designed," or similar language without any publicly named individual, credentials, or role.
What's in it
Plainly stated manufacturing stack: USA manufacture in FDA-registered facilities with cGMP compliance and a described Full Spectrum extraction process.
A genuinely built service layer: free Ask Our Experts (24–48h answers), a product finder, and an ailment index, all reachable from the hub.
Category conventions are followed honestly on the homeopathic side (dilution-and-format presentation).
What's not in it
The FAQ claims homeopathic medicines carry 'no risk of side effects or known interactions with pharmaceutical drugs' — a double absolute presented as fact.
The expert team is herbalists, naturopaths, and homeopaths — unnamed, and with no veterinarian mentioned anywhere for a pet-product line.
No evidence documents, named laboratory, COA, or per-active herbal amounts; condition- and outcome-named products (e.g., Kidney Support) imply outcomes nothing published supports.
Silver Star Brands, Inc., doing business as Native Remedies
Rebuilt research record for PetAlive from six live-fetched surfaces (2026-07-03): the hub, FAQ, Ask Our Experts, product finder, a flagship product page (Kidney Support, SKU 351...
Verified transparency record for Coco and Luna, re-fetched and re-scored on 2026-07-03 against the pet-supplement-brand-transparency-rubric-2026.2 tier anchors. Eleven public sources were crawled (one confirmed unreachable at a stale product URL, ten archived); every criterion below is grounded in a verbatim quote from a fetched, archived source, with gap text quoting the specific tier-anchor language that sets the score.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Active Identity Withheld
The brand uses proprietary blends, grouped amounts, or other label conventions that prevent a buyer from reading the per-active dose on at least one product in the line. Distinct from Line Inconsistency — captures the case where actives are hidden, not where products differ.
Evidence Buried
The brand technically publishes meaningful science, evidence, testing, or expert disclosure, but buyers cannot reach it without dedicated effort. Evidence that exists but is hard to find counts less.
What's in it
Ingredient names and short benefit or mechanism statements are directly visible on every live product page without requiring extra buyer effort.
A named individual (Caroline Hood) is publicly associated with veterinary approval of the product line, rather than an anonymous "our vet team" reference.
A manufacturing-quality claim naming FDA registration and GMP certification is publicly retrievable, even though it does not appear on the rendered product page.
What's not in it
No product in the crawled line discloses per-active ingredient amounts (mg, mcg, or IU) anywhere in buyer-visible text, image alt text, or structured data.
The site's recurring "clinical study" and "Clinically Researched Results" statistics carry no visible citation, link, author, or study name anywhere in the crawl.
No third-party laboratory, COA, or batch/lot testing language was found on any page checked, including the two pages most likely by title to carry it.
Verified transparency record for Coco and Luna, re-fetched and re-scored on 2026-07-03 against the pet-supplement-brand-transparency-rubric-2026.2 tier anchors. Eleven public so...
Plano Paws discloses more structural quality-system information than a first pass surfaces: a primary-navigation about page states the brand manufactures in a GMP compliant, FDA inspected US facility and asserts independent third-party testing. Facility identity, laboratory names, COAs, per-active dose amounts, and named expert review remain absent from the public record.
Public Evidence SystemNamed Vet ReviewerIngredient RationaleDisease-Claim-FreeNASC MemberFinished-Formula TrialNamed Mfg Facility
Worth Noting
Borrowed Evidence
The brand uses "clinically tested," "clinically proven," "study-backed," or trial-adjacent language without surfacing finished-formula or properly qualified ingredient-level evidence.
What's in it
The primary-navigation about page discloses a 'GMP compliant and FDA inspected facility' and an 'independent 3rd party testing' claim, repeated across multiple FAQ pages.
Official product pages name core joint, omega, and multivitamin ingredients with purpose-level rationale for each.
Fish oil pages disclose source fish, Icelandic sourcing, and molecular distillation language.
What's not in it
No named veterinarian, nutritionist, or formulator was found anywhere on the site, including the about page.
No public COA lookup, named laboratory, or lot-level report was found despite an explicit brand-wide third-party-testing claim.
No per-active dose amount or supplement-facts panel was found on any reviewed product across three product lines, and claim qualifier language ('may') is applied inconsistently between the flagship joint product and the multivitamin secondary line.
Plano Paws discloses more structural quality-system information than a first pass surfaces: a primary-navigation about page states the brand manufactures in a GMP compliant, FDA...