S. 1112 would make effective the proposed rule of the Food and Drug Administration relating to sunscreen drug products.
Detailed Summary
Sunscreen Labeling Protection Act of 2009 or the SUN Act - Requires the proposed rule issued by the Commissioner of Food and Drugs (FDA) pertaining to over-the-counter sunscreen drug products to take effect 180 days after enactment of this Act, unless the Commissioner issues a final rule that includes formulation, labeling, and testing requirements for both ultraviolet B (UVB) and ultraviolet A (UVA) radiation protection before such time.
Status of the Legislation
Latest Major Action: 5/20/2009: Referred to Senate committee. Status: Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
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