On the recordNovember 13, 2014
Mr. Speaker, I ask unanimous consent to take from the Speaker's table the bill (S. 2141) to amend the Federal Food, Drug, and Cosmetic Act to provide an alternative process for review of safety and effectiveness of nonprescription sunscreen active ingredients and for other purposes, and ask for its immediate consideration in the House. The Clerk read the title of the bill. The SPEAKER pro tempore. Is there objection to the request of the gentleman from Ohio? There was no objection. The text of the bill is as follows: S. 2141 Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled, SECTION 1. SHORT TITLE. This Act may be cited as the ``Sunscreen Innovation Act''. SEC. 2. REGULATION OF NONPRESCRIPTION SUNSCREEN ACTIVE INGREDIENTS. (a) In General.--Chapter V of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 351 et seq.) is amended by adding at the end the following: ``Subchapter I--Nonprescription Sunscreen and Other Active Ingredients ``SEC. 586. DEFINITIONS.…





