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    <number>4262</number>
    <updateDate>2019-11-15T21:18:14Z</updateDate>
    <updateDateIncludingText>2019-11-15T21:18:14Z</updateDateIncludingText>
    <originChamber>House</originChamber>
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    <type>HR</type>
    <introducedDate>2012-03-26</introducedDate>
    <congress>112</congress>
    <constitutionalAuthorityStatementText><![CDATA[<pre>From the Congressional Record Online through the Government Publishing Office [<a href='http://www.gpo.gov'>www.gpo.gov</a>]By Mr. PALLONE:H.R. 4262.Congress has the power to enact this legislation pursuantto the following:section 8 of article I of the Constitution.[Page H1571]</pre>]]></constitutionalAuthorityStatementText>
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        <title>MAP-21</title>
        <congress>112</congress>
        <number>14</number>
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          <actionDate>2012-03-21</actionDate>
          <text>Referred to the Committee on Transportation and Infrastructure, and in addition to the Committees on Ways and Means, Natural Resources, Energy and Commerce, Agriculture, Science, Space, and Technology, the Budget, Oversight and Government Reform, Financial Services, Education and the Workforce, and Foreign Affairs, 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.</text>
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        <text>Referred to the Subcommittee on Health.</text>
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        <text>Referred to the House Committee on Energy and Commerce.</text>
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        <bioguideId>P000034</bioguideId>
        <fullName>Rep. Pallone, Frank, Jr. [D-NJ-6]</fullName>
        <firstName>FRANK</firstName>
        <lastName>PALLONE</lastName>
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        <bioguideId>D000355</bioguideId>
        <fullName>Rep. Dingell, John D. [D-MI-15]</fullName>
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        <lastName>DINGELL</lastName>
        <party>D</party>
        <state>MI</state>
        <middleName>D.</middleName>
        <district>15</district>
        <sponsorshipDate>2012-03-26</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
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      <name>Health</name>
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    <summaries>
      <summary>
        <versionCode>00</versionCode>
        <actionDate>2012-03-26</actionDate>
        <actionDesc>Introduced in House</actionDesc>
        <updateDate>2012-06-06T20:10:54Z</updateDate>
        <text><![CDATA[ <p>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.</p> <p>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.</p> <p>Deems a cosmetic product adulterated if its manufacture, packing, or holding do not conform to current good manufacturing practice regulations.</p> <p>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.</p>]]></text>
      </summary>
    </summaries>
    <title>Cosmetics Safety Enhancement Act of 2012</title>
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        <titleType>Short Titles as Introduced</titleType>
        <title>Cosmetics Safety Enhancement Act of 2012</title>
      </item>
      <item>
        <titleType>Display Title</titleType>
        <title>Cosmetics Safety Enhancement Act of 2012</title>
      </item>
      <item>
        <titleType>Official Title as Introduced</titleType>
        <title>To amend the Federal Food, Drug, and Cosmetic Act to improve the safety of cosmetics.</title>
      </item>
    </titles>
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        <type>Introduced in House</type>
        <date>2012-03-26T04:00:00Z</date>
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            <url>https://www.govinfo.gov/content/pkg/BILLS-112hr4262ih/xml/BILLS-112hr4262ih.xml</url>
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    <latestAction>
      <actionDate>2012-03-30</actionDate>
      <text>Referred to the Subcommittee on Health.</text>
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    <dc:language>EN</dc:language>
    <dc:rights>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.</dc:rights>
    <dc:contributor>Congressional Research Service, Library of Congress</dc:contributor>
    <dc:description>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.</dc:description>
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