Marketing Magnesium: The Safe Way to Sell Relaxation Supplements
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…
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Compliance & Quality
COAs, FDA registration vs approval, GMP, DSHEA label requirements and third-party testing — supplement compliance explained for brand owners.
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Supplement Compliance 101: COAs, GMP, and FDA Rules Every Brand Owner Must Know
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.
Latest in Compliance & Quality
Prop 65 Warning: How to Legally Sell Supplements in California
Prop 65 supplement compliance comes down to heavy metal testing, correct warning labels, and knowing who enforces the law. This guide covers…
The Label Approval Myth: Why the FDA Won’t Check Your Artwork
No one at the FDA reviews your supplement label before launch. Learn the 6 required elements, how claims trigger misbranding risk, and…
Ingestible Beauty Profits: Cosmetic vs. Supplement Claims Explained
Cosmetic vs supplement claims follow different FDA paths. This guide explains the 4 claim types, what beauty brands can say about skin,…
Going Global: The Ultimate Guide to Selling Supplements Internationally
Selling supplements internationally means mastering DSHEA, Health Canada's NPN system, and EU food supplement rules before you ship a single bottle. Here…
Audit Your Manufacturer: The 5 Questions You Must Ask Before Launching
Audit any white label supplement manufacturer before launch with 5 questions on FDA registration, 21 CFR 111 GMP, batch COAs, and third-party…
Shield Your Assets: Why Every Supplement Startup Needs Liability Insurance
Your name on the label means manufacturer-level liability. Here are the 5 claims that hit supplement startups, what coverage costs, and how…
Surviving an FDA Warning Letter: The Creator’s Ultimate Survival Guide
An FDA warning letter can end a supplement brand fast, but most are survivable. Here are the disease claims that trigger enforcement,…
The Statement of Identity: How to Name Your Supplement Without FDA Penalties
The FDA statement of identity rule (21 CFR 101.3) decides how you name your supplement. Miss it and your product is misbranded.…
Made in the USA: The FTC Substantiation Trap You Must Avoid
FTC Made in USA supplement claims require proof the product is all or virtually all made in the US. Learn the labeling…
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