Free Guide
Compliance Quick-Start: COA + Label Requirements
The compliance questions every new supplement brand owner hits — answered in plain words, with examples you can copy.
- What a Certificate of Analysis is and how our per-LOT COA program works — every product, every batch, on demand
- Exactly what to do when Amazon, TikTok Shop, or a customer asks for documentation (a step-by-step response list)
- Every FDA-required label element explained in plain English — no regulatory jargon
- The claims line you cannot cross: 6 allowed-vs-not example pairs, plus 2 for skincare
- What FDA-registered, GMP, and third-party tested each actually mean
Trusted by brands · 3.5M+ units shipped · $200M+ in member revenue
Why it matters
Compliance is a trust asset, not a chore
Marketplaces will ask
Amazon and TikTok Shop routinely request product documentation. Brands that can answer in minutes keep listings live; brands that can’t, don’t.
One wrong claim is expensive
A single disease claim on a label or ad can trigger takedowns and regulator attention. The guide shows you the exact line — with side-by-side examples.
Credentials close sales
FDA-registered facility, GMP, per-LOT COAs — knowing what each means lets you answer customer trust questions with substance.