Address
304 North Cardinal St.
Dorchester Center, MA 02124
Work Hours
Monday to Friday: 7AM - 7PM
Weekend: 10AM - 5PM
Address
304 North Cardinal St.
Dorchester Center, MA 02124
Work Hours
Monday to Friday: 7AM - 7PM
Weekend: 10AM - 5PM
When working in the cosmetic packaging industry, you will get to know many friends in the cosmetics OEM industry, and in the process, you will also learn a lot of knowledge about this industry. Friends who have just entered the OEM industry and those who are engaged in cosmetics investment are all interested in the process of product filing. Below, Yusu Packaging will sort out the filing process and the materials that need to be prepared for general conventional products (non-imported, non-special purpose cosmetics), hoping to help everyone understand this process.
5. The entrusted production enterprise shall handle the registration of the entrusted processing products;
6. The same sales package that cannot be separated contains multiple products and has only one product name, which can be filed as one product;
7. The product specifications, models, formulas and production processes applied for filing are the same, but the trademarks or product names indicated on the product labels are different, and they should be filed separately for different products.
When applying for the registration of domestic non-special-purpose cosmetics, the following materials should be submitted:
1. Application form for the registration of domestic non-special-purpose cosmetics;
2. Basis for naming the product name;
3. Product formula (excluding content, except for restricted substances);
4. Brief description and diagram of the product production process;
5. List of product production equipment;
6. Product quality and safety control requirements;
7. Design and packaging of non-special cosmetics registration products (including product labels and product instructions);
8. Inspection reports and related materials issued by inspection agencies designated by provincial food and drug supervision and administration departments (hereinafter referred to as inspection agencies);
9. Relevant safety assessment materials for substances that may have safety risks in the product;
10. Copy of the health license of the production enterprise;
11. Copy of the health license of other entrusted parties (if there is entrusted production);
12. Copy of the entrusted production agreement (if there is entrusted production);
13. Other materials that may be helpful for registration.