PMG’s regulatory and labeling guides for supplement, skincare and OTC brands. Explore claims, registrations, testing and label requirements, with practical checklists for your launch.
Can a private label supplement or skincare product say Made in USA? The FTC’s 3-part test, qualified claims, California’s rule and a sourcing checklist.
How a spa or med spa launches its own skincare line: which claims make it a drug, what the label needs under MoCRA, professional-use rules and PMG minimums.
Does your private label supplement or skincare product need a Prop 65 warning? Who's responsible, what it must say, the 2025 short-form rules and a checklist.
What a supplement certificate of analysis must show under 21 CFR 111: methods, limits, actual results, identity and heavy metals, plus a printable checklist.
Certifications a supplement or skincare maker needs: what FDA requires, what NSF, USP and ISO 22716 audits prove, and organic, kosher, halal rules.
What a private label supplement label must include: 5 required statements, Supplement Facts rules, the claims disclaimer, allergens and adverse event contact.
Under MoCRA, the company named on a private label cosmetic's label is the responsible person. See who registers, lists and reports adverse events.
When a massage oil becomes an OTC drug: claims, FDA M017 menthol and camphor levels, child-resistant packaging, Drug Facts, minimums and timelines.
How claims set the FDA category, what Amazon hazmat review needs, when caps must be child-resistant, and PMG's minimums.
When an acne product becomes an OTC drug, which actives and strengths FDA’s acne monograph allows, Drug Facts labeling, NDCs and registration, what changes on the manufacturing floor, and realistic MOQs and timelines — plus a downloadable launch checklist.
