Summary Data on Registration and Listing of Cosmetic Facilities and Products
Recommendation
19/20 May 2026
All relevant GMP/GACP aspects for Medical Cannabis
On the Road to 30,000 Members
Let us become the World's Leading GMP/GDP Compliance Community in 2026
The FDA has provided summary data on the registration and listing of cosmetic product facilities and products.
Modernization of Cosmetics Regulation
Under the Modernization of Cosmetics Regulation Act of 2022 (MoCRA), manufacturers and processors of a cosmetic product for distribution in the United States must register their facilities with the FDA and renew their registration every two years. A responsible person must list each marketed cosmetic product with the FDA, including product ingredients, and provide any updates annually. There are exemptions, including for certain small businesses and for certain products and facilities that are subject to requirements for drugs and devices. The tabulated data is now available to the public on the FDA's Registration and Listing of Cosmetic Product Facilities and Products webpage.
For additional information on the FDA's registration and listing of cosmetic product facilities and products, please see:
- Guidance for Registration and Listing of Cosmetic Product Facilities and Products
- Additional Submission tools for Registration & Listing of Cosmetic Product Facilities and Products
Related GMP News
15.04.2026ICH Q9 Training Package updated
01.04.2026New EMA GMP Guidelines in the next three Years
01.04.2026New EMA Guidance: Risk Management for Elemental Impurities in Veterinary Medicinal Products
18.03.2026Sampling in the Focus of the FDA
11.03.2026EU Pharma Package: Final Texts officially published
11.03.2026FDA Guidance Plans for 2026