Features

Every check we run. Everything you get back.

90+ compliance checks across the CoA, label, listing, and cGMP certificate. Every finding cites its verbatim source line, includes the exact fix, and rolls up into an exportable report for each supplement.

The check catalog

Eight areas, mirroring how Amazon’s verification actually reads your documents.

Lab & Accreditation

12 checks
ISO/IEC 17025 accreditation body + certificate numberAmazon-approved TIC recognitionLab independence from manufacturerMethod of analysis (HPLC · AOAC · USP · EP)Authorized signature & titleFinished-product testing scopeManufacturer identification+ 5 more

Contaminants

14 checks
Heavy metals: Lead · Arsenic · Cadmium · MercuryThe N/A trap (non-numeric results)Heavy-metal limit exceedanceMicrobial panel: TAC · Yeast & Mold · E. coli · SalmonellaPathogen corrective-action pathPesticide residue panelCannabinoid contaminant screenProhibited adulterant detection+ 6 more

Ingredients & Potency

13 checks
Active ingredient match (synonym-aware)Active ingredient spec band (90–120%)Botanical identity testing (HPTLC · PCR · microscopy)Botanical Latin name & plant partExtract concentration ratioNutrient content toleranceOther ingredients listed+ 6 more

Dates & Traceability

9 checks
Lab report freshness (365-day window)Report date vs batch manufacture dateExpiration date logicBatch / lot number traceabilityLot number visible on labelCoA renewal advisory+ 3 more

Label rules

15 checks
21 CFR 101.93 FDA disclaimer — verbatim, both clausesDisclaimer placement, bolding & claim adjacencyDisease claim screeningProhibited label statementsNet quantity of contentsDirections for useServing size consistencyLabel image legibility+ 7 more

Listing cross-checks

16 checks
Listing potency vs CoA verificationListing potency vs Supplement Facts panelListing–SFP amount mismatch (>5% drift)Extract weight inflation (March 2026 policy)Product name match: listing vs CoA vs labelListing ingredient not on labelDisease claims in listing copy+ 9 more

cGMP & Facility

7 checks
21 CFR Part 111 certificate scopeFacility name & address matchCertificate expiryAnnual audit trackingCertifying body recognition+ 2 more

Policy & Claims

10 checks
Amazon TIC policy complianceProhibited FDA approval claimsDrug-equivalence claim detectionDrug-similar product name detectionHigh-risk category detectionProhibited supplement product forms+ 4 more

The rulebook stays current. Checks are updated continuously as Amazon and FDA policy evolves — new rules apply to your covered supplements automatically.

Everything you get back

The checks find the problems. This is what SuppGuard hands you to solve them — per supplement, in one dashboard.

Exportable reports

A full compliance report per supplement — findings, evidence, and fixes — exportable as a PDF for your team, supplier, or TIC.

Appeal letters

A pre-filled Amazon appeal built directly from your findings, ready to submit.

Lab email drafts

The exact request to send your lab — which lines to change and the quantitative format Amazon accepts.

Document vault

Every CoA, label, listing, and cGMP certificate stored securely and organized per SKU.

Expiry reminders

CoA freshness and cGMP audit windows tracked continuously — flagged well before they fail Amazon rules.

Re-checks on new batches

Upload a new batch and every finding re-runs automatically. Fixed issues clear; new ones surface.

Fast-Track recognition

Enrolled with NSF, USP, BSCG, Informed Sport, Clean Label, or GRMA? Declare it — no CoA upload needed.

Always-current rulebook

We track Amazon and FDA policy changes and update the checks for you — part of what “autopilot” means.

Common questions

What does a PASS actually mean?+

Document completeness and alignment with Amazon's supplement policy — not product safety or legal advice. SuppGuard is an administrative workflow tool: it tells you whether your paperwork will survive Amazon's verification, and what to fix if it won't.

What documents do I need?+

A Certificate of Analysis is the core document. Add the product label, Amazon listing text, and cGMP certificate to unlock label rules, cross-document checks, and facility checks. Fast-Track enrolled products don't need a CoA at all.

How fresh does my CoA need to be?+

Amazon rejects CoAs older than 365 days at submission, and the report date can't precede the batch manufacture date. SuppGuard tracks both and reminds you before the window closes.

How do you keep up when Amazon or the FDA changes the rules?+

Tracking policy is part of the product. When Amazon updates its supplement requirements or the FDA changes labeling rules, we update the check catalog — and every covered supplement is evaluated against the current rulebook, not the one from when you signed up.

My lab isn't one of Amazon's approved TIC organizations. Is my CoA useless?+

No. A CoA from any ISO/IEC 17025-accredited lab is valid evidence — it just routes through one of Amazon's approved TIC verifiers for submission. SuppGuard recognizes both lists and tells you which path your document is on.

Who is SuppGuard for?+

Supplement brands selling on Amazon, aggregators managing supplement portfolios, agencies and growth consultants who handle compliance for clients, and manufacturers who supply them. Anything with an ASIN and a Supplement Facts panel.

Is this legal or safety advice?+

No. Pass/Fail reflects document completeness and Amazon policy alignment only. SuppGuard is not affiliated with Amazon and does not provide legal, regulatory, or safety advice.

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