The draft legislation contains several provisions that will impact the beauty industry:
- Create an up-to-date registry of all cosmetic facilities serving American consumers. All facilities operating within the United States or exporting cosmetics to the United States would be required to register with the FDA annually. Registration would require payment of a $2,000 fee per facility.
- Require adverse event reporting. All cosmetic facilities would be required to report adverse events resulting from the use of their products to the FDA.
- All cosmetic facilities would be requird to comply with good manufacturing practices established by the Secretary of Health and Human Services.
- All importers of drugs, devices, foods and cosmetics would need to register with FDA annually and pay a registration fee. To improve the accuracy of data and the ability of FDA to identify more quickly parties involved in a crisis, facilities would be given a unique identification number.
- The FDA would be given additional resources to monitor foreign facilities producing food, drugs, devices and cosmetics for American consumers.