Requirements for filing the registration certificate of domestic non-special cosmetics:

1. The production enterprise is the 1 responsible person for product quality, safety and claimed functions, and is responsible for the authenticity of the filing materials and samples submitted by it, and bears corresponding legal responsibilities.

The food and drug administration of the United States does not conduct technical audits on the health and safety of products on record.

"Record Certificate" is not regarded as the recognition of product hygiene quality, and the enterprise shall not use the record certificate number as the publicity content.

2 change the product formula, product label identification, should be according to the new product for the record.

3. The same sales package contains multiple products with product names, and each product is filed separately.

Where the same product has multiple product specifications and models, the Registration Certificate of Domestic Cosmetics for Non-Special Use shall be filed separately.

4. The products entrusted for processing shall be put on record by the entrusted production enterprise.

5. The same undivided sales package contains multiple products with only one product name, which can be archived according to one product.

6. The product specifications, models, formulas and production processes applied for filing are the same, but the trademarks or product names marked on the product labels are different, so they should be filed separately according to different products.

To apply for the filing of domestic cosmetics for non-special purposes, the following materials shall be submitted:

1, application form for filing domestic non-special cosmetics

2. Naming basis of product name

3, product formula (excluding content, except restricted substances)

4. Brief description and sketch of product production process

5, product quality and safety control requirements

6, non-special cosmetics product design and packaging (including product labels, product manuals)

7. Inspection report and related materials issued by the inspection agency designated by the provincial food and drug supervision and administration department (hereinafter referred to as the inspection agency).

8. Relevant safety assessment data of safety risk substances that may exist in the product.

9. Copy of commissioned production agreement (if any)

10, and other information that may be helpful for filing.

Filing fee for entrusted processing of cosmetics

According to different products, the price is different, and the special products are relatively expensive.