Manufacturers’ OEM production of cosmetics requires filing
1. Filing conditions
Comply with the "Cosmetics Hygiene Supervision Regulations", "Cosmetics Hygiene Supervision Regulations Implementation Rules", " Basic requirements of "Hygienic Standards for Cosmetic Manufacturing Enterprises".
2. Submit information
1. "Application Form for Entrusted Production of Cosmetics"
2. Entrustment issued by the provincial and municipal cosmetics regulatory authorities where the entrusting party is located Production pre-registration notice and other supporting materials indicating that the provincial regulatory authorities have been notified. (This is not required if both entrusting parties are in this province)
3. The notarized entrusted production and processing contract signed by the entrusting party and the entrusted party and a copy of the notarial certificate (bring the original for verification). 4. Copies of the business licenses of the entrusting enterprise and the entrusted enterprise (bring the originals for verification);
5. Copies of the entrusted party's "Hygienic License for Cosmetics Production Enterprises" and "Cosmetics Production License";
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6. If you entrust the production of special-purpose cosmetics, you must provide a copy of the approval document for the special-purpose cosmetics (bring the original for verification);
7. The formula of the entrusted production product (excluding content, Except for restricted substances).
8. Entrust the production of labels and product instructions (samples) for cosmetics. The label instructions should comply with relevant regulations and should be marked with the names and addresses of both parties and the health license and production license number of the entrusted party. Those who produce special-purpose cosmetics should be marked with the special-purpose cosmetics approval number.
9. Product health, safety and quality management system documents between the entrusting party and the entrusted party;
10. When an applicant submits application materials, if the applicant is not the legal representative himself, he should submit "Letter of Authorization" and a copy of the applicant's ID card;
11. Other materials that the food and drug supervision and administration department deems should be provided.
3. Requirements and instructions for submitting information
1. Health laws, regulations, health standards and standards related to the application matters are the basis for application and approval. The applicant unit and relevant Personnel should read it carefully to ensure they understand their rights and obligations.
2. When filling in the name of the unit, the applicant should use the full name approved by the industrial and commercial administration department in accordance with the law; the product name should comply with the "Regulations on Naming Health-Related Products". The Chinese and English names of the products and the applicant's name in the application materials The names must be completely consistent. 3. All application materials must be printed on A4 size paper. It is recommended to use size 4 imitation Song characters for Chinese and size 12 characters for English. Arrange them in the order of the directory and stamp the official seal page by page before binding them into a volume. Submit the original information. One copy must be made, and the copy must be exactly the same as the original. ?
4. The application form needs to be printed and filled out on a computer. The filled-in content should be complete, clear, and must not be altered. Please mark "none" for matters that do not need to be declared, and no blank items are allowed; the applicant uses food from Hebei Province Fill out the application form downloaded from the Drug Administration website.
5. The same item in the application materials should be filled in consistently and should not be inconsistent. The name of the reporting unit should be consistent with its official seal.