Cosmetics Production License-CFDA,2017 Since January 1, 2017, the Cosmetics Production License has been unified. The original “National Industrial Product Production License” and “Health License for Cosmetic Manufacturing Enterprises” held by cosmetics manufacturing enterprises are automatically invalidated. Since January 1, 2017, no cosmetics manufacturing enterprise that has not obtained the Cosmetics Production License shall engage in the production of cosmetics. Cosmetic manufacturers with the original National Industrial Product Production License and the Health License for Cosmetic Manufacturing Enterprises can sell their products before December 31, 2016 to the end of their validity period. Cosmetics manufactured since July 1, 2017 must be labeled with a new packaging label with the information of the Cosmetic Production License. The following documents are required for application of hygiene license or record keeping certificate: Application form for license; Product ingredients; Effective components, evidence of use and inspection methods; Manufacturing technique and diagram; Product quality standard; Testing report from a cosmetics testing institution approved by the SFDA and related materials; Product package (sales package & product label); Certified document for production and sales in the manufacturing country (region); The statement on related problems of ‘Mad Cow Disease’;(new) Power of attorney, if responsible person has been appointed; SomeRead More →

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