S.4692

Homeopathic Drug Product Safety, Quality, and Transparency Act regulates homeopathic drug products under the Federal Food, Drug, and Cosmetic Act.

The Homeopathic Drug Product Safety, Quality, and Transparency Act amends the Federal Food, Drug, and Cosmetic Act to establish a regulatory framework for homeopathic drug products. It exempts these products from certain identity and strength testing requirements but mandates other final specifications like contaminant and defect testing. The Act creates a Homeopathic Drug Product Advisory Committee to advise on safety, quality, and labeling standards. It also mandates the Secretary of Health and Human Services to consult with the Committee on guidance and rulemaking.