China Cosmetic Production License Dossier Supplementation Requirements

To enhance cosmetic license review efficiency, Chinese Herbology Protection Review Committee requires applicants to conduct self-examination of cosmetic production license application dossiers. If dossiers are incomplete, timely supplementation with additional documentation is mandatory.

1. Applicants who have applied for administrative licensing but have not submitted relevant documents relating to production license and have not yet been issued an administrative decision by SAMR (former CFDA) should submit supplementary documents to Chinese Herbology Protection Review Committee as soon as possible.

2. If the name of the cosmetic company listed on the new "Cosmetic Production License" differs from that on the old one (caused by the change of format), the company should submit the copy of the "Cosmetic Production License" and the certificate of "Actual Production Spot remains the same" issued by local FDA.

3. Cosmetic companies that have changed production location/address should submit the copy of "Cosmetic Production License" and supplement related documents in accordance with the corresponding requirements in "Requirements for Application and Acceptance of Administrative Licensing for Cosmetics".

4. When submitting supplementary documentation the corresponding product name and application number should be specified.

5. All documents can be mailed directly to Cosmetic Division, Chinese Herbology Protection Review Committee. The address is Building 12, Section 11, Nansihuan (the South Fourth Ring Road), Xilu (West Road), Beijing.