Rulemaking and interagency coordination

(a) Regulations Not later than 1 year after the date of enactment of this Act, the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, in consultation with the Consumer Product Safety Commission and the Federal Trade Commission, shall issue regulations to carry out section 569E of the Federal Food, Drug, and Cosmetic Act, as added by section 3. (b) Annual reporting Not later than October 31, 2027, and annually thereafter, the Secretary of Health and Human Services, in consultation with the Commissioner of Food and Drugs, shall submit a report on enforcement actions, public health outcomes, and recommendations for policy updates relating to the regulation of nitrous oxide products, as defined in section 569E of the Federal, Food, Drug, and Cosmetic Act, as added by section 3, including pursuant to section 569E of the Federal Food, Drug, and Cosmetic Act (as added by section 3), to— (1) the Committee on Health, Education, Labor, and Pensions, the Committee on Commerce, Science, and Transportation, and the Committee on the Judiciary of the Senate; and (2) the Committee on Energy and Commerce and the Committee on the Judiciary of the House of Representatives.