Last 7 August the FDA has published a draft that will serve as a guide for the future registration of facilities and listing of cosmetic products, applicable to all those companies that manufacture and distribute this type of goods in the United States.
In this guide it is described as, first of all, FDA intends to apply for FDA Establishment Identifier (FEI) as installation registration number, and gives the necessary keys to obtain it by the responsible person in each company.
This registration number will allow organizations to present the list of products that they want to market or that are already on the market.. In this sense, The FDA establishes a series of deadlines for listing:
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The person responsible for a cosmetic product that is marketed on 29 from December to 2022, must submit a list of cosmetic products no later than 29 from December to 2023,
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or for a cosmetic product that is placed on the market for the first time after 29 from December to 2022, within the 120 days after said product is marketed in interstate commerce.
Besides, The responsible person must report annually any update within the list of communicated products..
Some of the data required for the registration of products will be the following:
- FDA Establishment Identifier (FEI)
- Contact details of the responsible person
- Category of the cosmetic product to be listed
- List of ingredients
Please Note MoCRA Exempts Certain Small Businesses from Facility Registration and Product Listing Requirements.
Once the final legislation is published, From Burotec we can help you carry out the registration of your facilities, as well as the list of your products, thereby ensuring full compliance with US legislation.
