Purchase the item on this page to register your foreign cosmetic facility and have FDA Solutions Group, LLC serve as your U.S. Agent for 2024 - 2025, if you do not already have such an agent.
As part of facility registration, FDA Solutions Group will determine if the facility has a Firm Establishment Identifier (FEI). If the facility does not have a FEI, this registration will initiate creation of a FEI number.
If any facility information changes after purchase, the company must provide the changes to FDA Solutions Group as soon as possible.
FDA Solutions Group will provide an electronic certificate of completion upon request.
Cosmetic Facility Registration Requirement
With the passing of MoCRA, FDA requires biennial registration renewal between October 1 and December 31 of every odd-numbered year.
The FDA requires all foreign facilities that engage in the manufacturing or processing of a cosmetic product for distribution in the United States to register with the FDA and designate a U.S. Agent. The U.S. Agent is a person or entity located within, or that maintains an office in, the United States. The U.S. Agent plays the role of the domestic representative for the foreign facility through which all communication with the FDA takes place.
Additionally, all cosmetic products must be listed with the FDA. Learn about our cosmetic product listing service.