Senior Regulatory Counsel

0910-AG59 201510 The Regulatory Plan and the Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Requirements for the Testing and Reporting of Tobacco Product Constituents, Ingredients, and Additives

The Federal Food, Drug, and Cosmetic Act, as amended by the Family Smoking Prevention and Tobacco Control Act, requires the Food and Drug Administration to promulgate regulations that require the testing and reporting of tobacco product constituents, ingredients, and additives, including smoke constituents, that the Agency determines should be tested to protect the public health.

]]> Economically Significant Previously Published in The Unified Agenda Proposed Rule Stage Yes Private Sector Not Yet Determined 21 U.S.C. 301 et seq. 21 U.S.C. 387 The Family Smoking Prevention and Tobacco Control Act Statutory Final 04/00/2013 sec 915(a) of the Federal Food, Drug, and Cosmetic Act Final rule must be issued no later than 36 months after April 1, 2010--see section 915(a) of the Federal Food, Drug, and Cosmetic Act and section 6 of the Family Smoking Prevention and Tobacco Control Act. No NPRM 07/00/2016 Yes Businesses Undetermined Undetermined No Yes No Laura Rich Senior Regulatory Counsel 0910 Food and Drug Administration FDA 877 287-1373 ctpregulations@fda.hhs.gov Center for Tobacco Products, 10903 New Hampshire Avenue, Building 71, Room G335, Silver Spring MD 20993