The US Food and Drug Administration has updated its guidance for registering cosmetic manufacturing facilities and listing products under the Modernization of Cosmetics Regulation Act to include three new Q&A items that will provide clarification on the responsibilities of US agents, the use of a single identifier number for multiple facilities and the listing of samples and gifts within the regulation’s portal.
US FDA Updates MoCRA Registration Guidance To Answer Stakeholder Questions
FDA publishes an updated registration guidance in the Federal Register 12 December to answer outstanding questions by stakeholders, including whether a single FEI number can be used for multiple related facilities.
More from Compliance
More from HBW Insight
• By
Tariffs on imports from China and look at eliminating self-affirmed GRAS pathway introduced under Trump while DoJ Consumer Protection Branch also continues supplement sector priorities enduring across administrations.
• By
Round up of the latest appointments: PAGB names vice presidents; Activ'Inside gets first US head; EMA elects management board chair.
• By
Data from the US Food and Drug Administration indicated that two hair dye ingredients are formulated in eye makeup and dermal application products, prompting a Cosmetic Ingredient Review panel to conclude one dye is unsafe for such uses and discouraging those uses in the other dye.