Cancer-Free Label Act of 2012

Summary

Cancer-Free Label Act of 2012 - Directs the head of each federal agency that regulates a covered product to establish a program to permit the labeling of such a product that does not contain any carcinogens as "Cancer-Free." Defines a "covered product" to mean any product offered for sale that is: (1) regulated by the Food and Drug Administration (FDA), the Environmental Protection Agency (EPA), the Department of Agriculture (USDA), or the Consumer Product Safety Commission (CPSC); and (2) intended for individual or residential use. Requires such agency heads to coordinate to develop an easily recognizable label: (1) to be affixed to a covered product to signify that it has been approved for "Cancer-Free" labeling, and (2) to include a notice stating that "This product does not contain known or likely carcinogens that increase your risk of cancer." Prohibits the introduction or offering for introduction into interstate commerce of a covered product affixed with a "Cancer-Free" label if: (1) the head of each federal agency that regulates the product has not approved an application for the labeling of the product as "Cancer-Free," or (2) the product contains any substance that is not listed in such application. Sets forth requirements regarding: (1) application approval and confidentiality; (2) random testing of covered products, random audits of facilities in which such products are manufactured, and measures to ensure compliance with agency guidance; (3) application fees; and (4) penalties for violations. Requires such agency heads to: (1) issue guidance to prevent the introduction of carcinogens into such product during its manufacture, storage, and transportation; and (2) post on the agency's public website a list of all covered products regulated by that agency that have been approved for labeling as "Cancer-Free."

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Timeline

1. 25 July 2012

   Introduced

   Referred to the Committee on Energy and Commerce, and in addition to the Committee on Agriculture, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.

   Source: IntroReferral

2. 25 July 2012

   Introduced

   Sponsor introductory remarks on measure. (CR H5212, E1320)

   Source: IntroReferral

3. 25 July 2012

   Introduced

   Introduced in House

   Source: IntroReferral

4. 25 July 2012

   Introduced

   Introduced in House

   Source: IntroReferral

5. 27 July 2012

   Referred

   Referred to the Subcommittee on Health.

   Source: Committee

6. 13 August 2012

   Referred

   Referred to the Subcommittee on Nutrition and Horticulture .

   Source: Committee

Votes

No vote records are attached yet.

Versions

• Introduced in House · 25 July 2012 · Download file

Documents

3 official files

• Introduced in House (text)

  Introduced in House · EN · 25 July 2012

  ViewDownloadOpen at official source

• Introduced in House (PDF)

  Introduced in House · EN · 25 July 2012

  ViewDownloadOpen at official source

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• Introduced in House

  summary · EN · 25 July 2012

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  Vertaal naarNL · DutchDE · GermanFR · FrenchES · SpanishIT · ItalianPL · PolishPT · PortugueseSV · SwedishDA · DanishFI · FinnishEL · GreekCS · CzechHU · HungarianRO · RomanianBG · BulgarianHR · CroatianSK · SlovakSL · SlovenianLT · LithuanianLV · LatvianET · EstonianGA · IrishMT · Maltese

  Vertaal document

  Documentvertaling op verzoek met downloadbare PDF (logo + link naar de officiële bron). Het bronbestand blijft leidend.

Sponsors

• Rep. Deutch, Theodore E. [D-FL-22] · D · Sponsor
• · hsag00 · Standing
• · hsif00 · Standing

Related records

• related to ← Carcinogen-Free Label Act of 2012