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    <number>2132</number>
    <updateDate>2019-11-15T21:21:16Z</updateDate>
    <updateDateIncludingText>2019-11-15T21:21:16Z</updateDateIncludingText>
    <originChamber>House</originChamber>
    <originChamberCode>H</originChamberCode>
    <type>HR</type>
    <introducedDate>2011-06-03</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 Mrs. LOWEY:H.R. 2132.Congress has the power to enact this legislation pursuantto the following:Article I[[Page H4037]][Page H4036]</pre>]]></constitutionalAuthorityStatementText>
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        <name>Energy and Commerce Committee</name>
        <chamber>House</chamber>
        <type>Standing</type>
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            <systemCode>hsif14</systemCode>
            <name>Health Subcommittee</name>
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                <name>Referred to</name>
                <date>2011-06-03T18:37:37Z</date>
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        <activities>
          <item>
            <name>Referred to</name>
            <date>2011-06-03T13:01:20Z</date>
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        </activities>
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    </committees>
    <relatedBills>
      <item>
        <title>SUN Act</title>
        <congress>112</congress>
        <number>1064</number>
        <type>S</type>
        <latestAction>
          <actionDate>2011-05-25</actionDate>
          <text>Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S3344)</text>
        </latestAction>
        <relationshipDetails>
          <item>
            <type>Related bill</type>
            <identifiedBy>CRS</identifiedBy>
          </item>
        </relationshipDetails>
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    </relatedBills>
    <actions>
      <item>
        <actionDate>2011-06-03</actionDate>
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            <name>Health Subcommittee</name>
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        </committees>
        <sourceSystem>
          <code>1</code>
          <name>House committee actions</name>
        </sourceSystem>
        <text>Referred to the Subcommittee on Health.</text>
        <type>Committee</type>
      </item>
      <item>
        <actionDate>2011-06-03</actionDate>
        <text>Referred to the House Committee on Energy and Commerce.</text>
        <type>IntroReferral</type>
        <actionCode>H11100</actionCode>
        <sourceSystem>
          <code>2</code>
          <name>House floor actions</name>
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            <systemCode>hsif00</systemCode>
            <name>Energy and Commerce Committee</name>
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        <actionDate>2011-06-03</actionDate>
        <text>Introduced in House</text>
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        <actionDate>2011-06-03</actionDate>
        <text>Introduced in House</text>
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          <code>9</code>
          <name>Library of Congress</name>
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    <sponsors>
      <item>
        <bioguideId>L000480</bioguideId>
        <fullName>Rep. Lowey, Nita M. [D-NY-18]</fullName>
        <firstName>NITA</firstName>
        <lastName>LOWEY</lastName>
        <party>D</party>
        <state>NY</state>
        <middleName>M.</middleName>
        <district>18</district>
        <isByRequest>N</isByRequest>
      </item>
    </sponsors>
    <cosponsors>
      <item>
        <bioguideId>I000057</bioguideId>
        <fullName>Rep. Israel, Steve [D-NY-2]</fullName>
        <firstName>STEVE</firstName>
        <lastName>ISRAEL</lastName>
        <party>D</party>
        <state>NY</state>
        <district>2</district>
        <sponsorshipDate>2011-06-03</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
      </item>
    </cosponsors>
    <policyArea>
      <name>Health</name>
    </policyArea>
    <subjects>
      <legislativeSubjects>
        <item>
          <name>Administrative law and regulatory procedures</name>
        </item>
        <item>
          <name>Cancer</name>
        </item>
        <item>
          <name>Consumer affairs</name>
        </item>
        <item>
          <name>Department of Health and Human Services</name>
        </item>
        <item>
          <name>Drug safety, medical device, and laboratory regulation</name>
        </item>
        <item>
          <name>Food and Drug Administration (FDA)</name>
        </item>
        <item>
          <name>Government information and archives</name>
        </item>
        <item>
          <name>Health information and medical records</name>
        </item>
        <item>
          <name>Medical research</name>
        </item>
        <item>
          <name>Musculoskeletal and skin diseases</name>
        </item>
      </legislativeSubjects>
      <policyArea>
        <name>Health</name>
      </policyArea>
    </subjects>
    <summaries>
      <summary>
        <versionCode>00</versionCode>
        <actionDate>2011-06-03</actionDate>
        <actionDesc>Introduced in House</actionDesc>
        <updateDate>2011-06-29T20:39:43Z</updateDate>
        <text><![CDATA[ <p>Skin Cancer Prevention, Education, and Consumer Right-To-Know Act - Requires the proposed rule issued by the Commissioner of Food and Drugs (FDA) pertaining to over-the-counter sunscreen drug products to take effect 180 days after enactment of this Act, unless the Commissioner issues a final rule that includes formulation, labeling, and testing requirements for both ultraviolet B (UVB) and ultraviolet A (UVA) radiation protection before such time.</p> <p>Directs the Secretary of Health and Human Services (HHS) to implement a general, nationwide education campaign identifying the risks posed by sun exposure without the use of a sunscreen providing broad-spectrum protection.</p>]]></text>
      </summary>
    </summaries>
    <title>Skin Cancer Prevention, Education, and Consumer Right-To-Know Act</title>
    <titles>
      <item>
        <titleType>Short Titles as Introduced</titleType>
        <title>Skin Cancer Prevention, Education, and Consumer Right-To-Know Act</title>
      </item>
      <item>
        <titleType>Display Title</titleType>
        <title>Skin Cancer Prevention, Education, and Consumer Right-To-Know Act</title>
      </item>
      <item>
        <titleType>Official Title as Introduced</titleType>
        <title>To require the Food and Drug Administration to finalize a standard for broad-spectrum protection in sunscreen products, and for other purposes.</title>
      </item>
    </titles>
    <textVersions>
      <item>
        <type>Introduced in House</type>
        <date>2011-06-03T04:00:00Z</date>
        <formats>
          <item>
            <url>https://www.govinfo.gov/content/pkg/BILLS-112hr2132ih/xml/BILLS-112hr2132ih.xml</url>
          </item>
        </formats>
      </item>
    </textVersions>
    <latestAction>
      <actionDate>2011-06-03</actionDate>
      <text>Referred to the Subcommittee on Health.</text>
    </latestAction>
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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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