FDA is requesting public comments on proposed information collection requirements for cosmetic product facility registration and product listing under the Federal Food, Drug, and C
The FDA has issued draft guidance on registration and listing requirements for cosmetic product facilities and products under the Modernization of Cosmetics Regulation Act (MoCRA).
The FDA has proposed a rule that would require testing methods for detecting and identifying asbestos in talc-containing cosmetic products. If finalized, manufacturers would need t
The FDA has issued final guidance on tattoo inks, which may affect manufacturers and distributors of these products. The guidance likely clarifies regulatory expectations, but spec
The FDA has issued a draft guidance on registration and listing requirements for cosmetic product facilities and products under the Modernization of Cosmetics Regulation Act (MoCRA
FDA has issued a compliance policy guide addressing registration and listing obligations under MoCRA. The document outlines FDA’s enforcement approach for cosmetic facility registr
The FDA has issued a draft guidance on cosmetic Good Manufacturing Practices (GMP). This draft outlines proposed requirements for manufacturing, processing, packing, and holding co
The FDA has issued a draft guidance on its authority to access records related to cosmetic products. Comments are due by March 23, 2026. The guidance clarifies the criteria, proces
FDA is seeking public comments on topics related to cosmetics regulation to prepare for the ICCR-20 meeting in Tokyo, Japan, July 7-9, 2026. Comments must be submitted by May 18, 2
Aprinnova LLC has proposed to produce cosmetic products, including squalane, Hydrogenated Poly (C6-20 Olefin), and Hydrogenated Difarnesene, at its facility in Leland, North Caroli