H.R. 4262 (112th): Cosmetics Safety Enhancement Act of 2012

Introduced:
Mar 26, 2012 (112th Congress, 2011–2013)
Status:
Died (Referred to Committee) in a previous session of Congress

This bill was introduced on March 26, 2012, in a previous session of Congress, but was not enacted.

Introduced
Mar 26, 2012
 
Sponsor
Frank Pallone Jr.
Representative for New Jersey's 6th congressional district
Party
Democrat
Text
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Last Updated
Mar 26, 2012
Length
38 pages
Related Bills
H.R. 14 (Related)
MAP-21

Referred to Committee
Last Action: Mar 21, 2012

 
Full Title

To amend the Federal Food, Drug, and Cosmetic Act to improve the safety of cosmetics.

Summary

No summaries available.

 
Cosponsors
1 cosponsors (1D) (show)
Committees

House Energy and Commerce

Health

The committee chair determines whether a bill will move past the committee stage.

 
Primary Source

THOMAS.gov (The Library of Congress)

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Notes

H.R. stands for House of Representatives bill.

A bill must be passed by both the House and Senate in identical form and then be signed by the president to become law.

The bill’s title was written by its sponsor.

GovTrack’s Bill Summary

We don’t have a summary available yet.

Library of Congress Summary

The summary below was written by the Congressional Research Service, which is a nonpartisan division of the Library of Congress.


3/26/2012--Introduced.
Cosmetics Safety Enhancement Act of 2012 - Amends the the Federal Food, Drug, and Cosmetic Act to require the registration of cosmetic products and cosmetic manufacturing facilities, including, for each product: (1) a unique facility identifier, (2) every product's brand name, and (3) product ingredients. Sets registration fees.
Requires a cosmetic manufacturer:
(1) before the introduction into interstate commerce of a cosmetic product, to establish a file containing scientific evidence substantiating the product's safety;
(2) to report any serious adverse event information received that is associated with the use of a cosmetic product; and
(3) maintain records concerning any cosmetic product that may be adulterated, misbranded, or otherwise in violation of the Act, including all records relating to cosmetic product safety substantiation or relating to serious adverse event reports.
Deems a cosmetic product adulterated if its manufacture, packing, or holding do not conform to current good manufacturing practice regulations.
Provides each manufacturer with an opportunity to cease distribution and recall of a cosmetic product if it is determined that there is a reasonable probability that the product is adulterated and the use of, or exposure to, such product will cause serious adverse health consequences or death to humans. Permits the issuance of an order requiring a recall if there is not a voluntary recall of an adulterated product.

House Republican Conference Summary

The summary below was written by the House Republican Conference, which is the caucus of Republicans in the House of Representatives.


No summary available.

House Democratic Caucus Summary

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