3.0.0 4083 2023-01-11T20:16:29Z 2023-01-11T20:16:29Z House H HR 2007-11-06 110 hsif00 Energy and Commerce Committee House Standing Referred to 2007-11-06T14:01:00Z Non-Prescription Drug Modernization Act of 2007 110 2311 S 2007-11-06 Read twice and referred to the Committee on Health, Education, Labor, and Pensions. Identical bill CRS 2007-11-06 Referred to the House Committee on Energy and Commerce. IntroReferral H11100 2 House floor actions hsif00 Energy and Commerce Committee 2007-11-06 Introduced in House IntroReferral Intro-H 9 Library of Congress 2007-11-06 Introduced in House IntroReferral 1000 9 Library of Congress W000215 Rep. Waxman, Henry A. [D-CA-30] HENRY WAXMAN D CA A. 30 N A000357 Rep. Allen, Thomas H. [D-ME-1] THOMAS ALLEN D ME H. 1 2007-11-06 True M000725 Rep. Miller, George [D-CA-7] GEORGE MILLER D CA 7 2007-12-06 False C001036 Rep. Capps, Lois [D-CA-23] LOIS CAPPS D CA 23 2007-12-11 False D000197 Rep. DeGette, Diana [D-CO-1] DIANA DEGETTE D CO 1 2007-12-11 False C001068 Rep. Cohen, Steve [D-TN-9] Steve Cohen D TN 9 2007-12-19 False L000551 Rep. Lee, Barbara [D-CA-9] BARBARA LEE D CA 9 2008-03-10 False Health Administrative procedure Commerce Congress Congressional reporting requirements Consumer education Deceptive advertising Department of Health and Human Services Drug adulteration Drug industry Drugs Food and Drug Administration (FDA) Government Operations and Politics Labeling Law Health 00 2007-11-06 Introduced in House 2008-03-04T21:21:09Z Non-Prescription Drug Modernization Act of 2007 - Amends the Federal Food, Drug, and Cosmetic Act to authorize: (1) the amendment or repeal of an over-the-counter drug monograph without notice and public procedure if there is a finding by the Secretary of Health and Human Services that a category of drugs or a specific drug is associated with a significant risk or that such drugs lack evidence of effectiveness; and (2) the Food and Drug Administration (FDA) to regulate over-the-counter drug advertisements.

Directs the Commissioner of Food and Drugs to identify over-the-counter drug monographs that may require amendment or repeal and to report the findings to Congress.

]]> Non-Prescription Drug Modernization Act of 2007 Official Title as Introduced To amend the Federal Food, Drug, and Cosmetic Act to provide for the amendment or repeal of monographs, to expand the Food and Drug Administration's authority to regulate drug advertising, and for other purposes. Introduced in House IH Display Title Non-Prescription Drug Modernization Act of 2007 Short Titles as Introduced Non-Prescription Drug Modernization Act of 2007 Introduced in House 2007-11-06T05:00:00Z https://www.govinfo.gov/content/pkg/BILLS-110hr4083ih/xml/BILLS-110hr4083ih.xml 2007-11-06 Referred to the House Committee on Energy and Commerce. text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. Congressional Research Service, Library of Congress This file contains bill summaries and statuses for federal legislation. A bill summary describes the most significant provisions of a piece of legislation and details the effects the legislative text may have on current law and federal programs. Bill summaries are authored by the Congressional Research Service (CRS) of the Library of Congress. As stated in Public Law 91-510 (2 USC 166 (d)(6)), one of the duties of CRS is "to prepare summaries and digests of bills and resolutions of a public general nature introduced in the Senate or House of Representatives". For more information, refer to the User Guide that accompanies this file.