Implementation of the sunscreen provisions in the reauthorization of the Food and Drug Administration (FDA) Over-the-Counter Monograph User Fee Act (OMUFA); FDA proposed order on OTC sunscreen active ingredients; sunscreen provisions in the Fiscal Year 2027 appropriations for the Food and Drug Administration; use of sunscreen in schools to prevent sunburns in children; FDA policy on animal testing for over-the-counter drugs; FDA Modernization Act 3.0 (S. 355; H.R. 2821).
Government entities lobbied:Food & Drug Administration (FDA); HOUSE OF REPRESENTATIVES; SENATE
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