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    <number>1586</number>
    <updateDate>2023-01-11T13:35:36Z</updateDate>
    <updateDateIncludingText>2023-01-11T13:35:36Z</updateDateIncludingText>
    <originChamber>House</originChamber>
    <type>HR</type>
    <introducedDate>2017-03-16</introducedDate>
    <congress>115</congress>
    <constitutionalAuthorityStatementText><![CDATA[<pre>[Congressional Record Volume 163, Number 46 (Thursday, March 16, 2017)]From the Congressional Record Online through the Government Publishing Office [<a href='http://www.gpo.gov'>www.gpo.gov</a>]By Mr. SERRANO:H.R. 1586.Congress has the power to enact this legislation pursuantto the following:Article I, Section 8 of the United States Constitution[Page H2150]</pre>]]></constitutionalAuthorityStatementText>
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        <chamber>House</chamber>
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            <name>Health Subcommittee</name>
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            <name>Referred to</name>
            <date>2017-03-16T14:01:15Z</date>
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        <actionDate>2017-03-17</actionDate>
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        <text>Referred to the Subcommittee on Health.</text>
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        <actionDate>2017-03-16</actionDate>
        <text>Referred to the House Committee on Energy and Commerce.</text>
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    <sponsors>
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        <bioguideId>S000248</bioguideId>
        <fullName>Rep. Serrano, Jose E. [D-NY-15]</fullName>
        <firstName>JOSE</firstName>
        <lastName>SERRANO</lastName>
        <party>D</party>
        <state>NY</state>
        <middleName>E.</middleName>
        <district>15</district>
        <isByRequest>N</isByRequest>
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    <policyArea>
      <name>Health</name>
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    <subjects>
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          <name>Administrative law and regulatory procedures</name>
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          <name>Child health</name>
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          <name>Department of Health and Human Services</name>
        </item>
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          <name>Drug safety, medical device, and laboratory regulation</name>
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          <name>Food and Drug Administration (FDA)</name>
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        <name>Health</name>
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        <actionDate>2017-03-16</actionDate>
        <actionDesc>Introduced in House</actionDesc>
        <updateDate>2017-07-13T13:18:10Z</updateDate>
        <text><![CDATA[ <p><b>Protecting Our Kids' Medicine Act of 2017</b></p> <p>This bill amends the Federal Food, Drug, and Cosmetic Act to prohibit the sale of liquid formulations of over-the-counter drugs that are not packaged with a dosage delivery device, such as a calibrated cup or spoon, and that do not have measurements on the label and on the dosage delivery device exclusively in metric units. The Food and Drug Administration may waive the requirement for metric units if that requirement would not benefit public health.</p> Over-the-counter liquid drugs labeled for pediatric use may not be sold without a flow restrictor or another mechanism to reduce accidental ingestion.]]></text>
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    <title>Protecting Our Kids' Medicine Act of 2017</title>
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        <titleType>Display Title</titleType>
        <title>Protecting Our Kids' Medicine Act of 2017</title>
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        <titleType>Official Title as Introduced</titleType>
        <title>To amend the Federal Food, Drug, and Cosmetic Act to ensure that liquid over-the-counter medications are packaged with appropriate dosage delivery devices and, in the case of such medications labeled for pediatric use, appropriate flow restrictors, and for other purposes.</title>
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        <title>Protecting Our Kids' Medicine Act of 2017</title>
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        <type>Introduced in House</type>
        <date>2017-03-16T04:00:00Z</date>
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            <url>https://www.govinfo.gov/content/pkg/BILLS-115hr1586ih/xml/BILLS-115hr1586ih.xml</url>
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    <latestAction>
      <actionDate>2017-03-17</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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