COAs, FDA registration vs approval, GMP, DSHEA label requirements and third-party testing — supplement compliance explained for brand owners.
Coming soon
The flagship guide for this topic is in production. In the meantime, the latest articles below get you moving — or browse everything on the blog.
Magnesium glycinate is a high-demand white-label category, but one banned word can sink a brand. Learn FDA-safe structure/function language, substantiation rules, and…
Prop 65 supplement compliance comes down to heavy metal testing, correct warning labels, and knowing who enforces the law. This guide covers…
No one at the FDA reviews your supplement label before launch. Learn the 6 required elements, how claims trigger misbranding risk, and…
Cosmetic vs supplement claims follow different FDA paths. This guide explains the 4 claim types, what beauty brands can say about skin,…
Selling supplements internationally means mastering DSHEA, Health Canada's NPN system, and EU food supplement rules before you ship a single bottle. Here…
Audit any white label supplement manufacturer before launch with 5 questions on FDA registration, 21 CFR 111 GMP, batch COAs, and third-party…
Your name on the label means manufacturer-level liability. Here are the 5 claims that hit supplement startups, what coverage costs, and how…
An FDA warning letter can end a supplement brand fast, but most are survivable. Here are the disease claims that trigger enforcement,…
The FDA statement of identity rule (21 CFR 101.3) decides how you name your supplement. Miss it and your product is misbranded.…
FTC Made in USA supplement claims require proof the product is all or virtually all made in the US. Learn the labeling…
Pick from 146 products, put your label on them, and we fulfill every order from our Georgia fulfillment center — no inventory, no minimums.
