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<bill bill-stage="Introduced-in-House" bill-type="olc" dms-id="H3550B8A19E594BC49527E707C2E18CB9" key="H" public-private="public"><metadata xmlns:dc="http://purl.org/dc/elements/1.1/">
<dublinCore>
<dc:title>115 HR 6047 IH: Synthetic Abuse and Labeling of Toxic Substances Act of 2018</dc:title>
<dc:publisher>U.S. House of Representatives</dc:publisher>
<dc:date>2018-06-07</dc:date>
<dc:format>text/xml</dc:format>
<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>
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<distribution-code display="yes">I</distribution-code><congress display="yes">115th CONGRESS</congress><session display="yes">2d Session</session><legis-num display="yes">H. R. 6047</legis-num><current-chamber>IN THE HOUSE OF REPRESENTATIVES</current-chamber><action display="yes"><action-date date="20180607">June 7, 2018</action-date><action-desc><sponsor name-id="T000238">Mr. Thornberry</sponsor> introduced the following bill; which was referred to the <committee-name committee-id="HIF00">Committee on Energy and Commerce</committee-name>, and in addition to the <committee-name committee-id="HJU00">Committee on the Judiciary</committee-name>, 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</action-desc></action><legis-type>A BILL</legis-type><official-title display="yes">To amend the Controlled Substances Act relating to controlled substance analogues.</official-title></form>
	<legis-body id="H2B5E4FD7731E4A4095A5195176802A88" style="OLC">
 <section id="H463ED8AB1A1247C2ACAFACF86E2C99AB" section-type="section-one"><enum>1.</enum><header>Short title</header><text display-inline="no-display-inline">This Act may be cited as the <quote><short-title>Synthetic Abuse and Labeling of Toxic Substances Act of 2018</short-title></quote> or the <quote><short-title>SALTS Act</short-title></quote>.</text> </section><section id="H2E88EDD97D7F4A8FBC09560892F201FD" section-type="subsequent-section"><enum>2.</enum><header>Controlled substance analogues</header><text display-inline="no-display-inline">Section 203 of the Controlled Substances Act (<external-xref legal-doc="usc" parsable-cite="usc/21/813">21 U.S.C. 813</external-xref>) is amended—</text>
 <paragraph id="H3AF2D1A4843A46699F8721CFFD0CCAAE"><enum>(1)</enum><text>by striking <quote>A controlled</quote> and inserting <quote>(a) <header-in-text level="subsection" style="OLC">In general</header-in-text>.—A controlled</quote>; and</text> </paragraph><paragraph id="H998F43FAD08C43888E43D36A26B7F25D"><enum>(2)</enum><text>by adding at the end the following:</text>
				<quoted-block display-inline="no-display-inline" id="HA3FC2CEE908344DE8BC3061B1F2EE080" style="OLC">
 <subsection id="H89C29D31C10143DEA09EC8205F693390"><enum>(b)</enum><header>Determination</header><text>In determining whether a controlled substance analogue was intended for human consumption under subsection (a), the following factors may be considered, along with any other relevant factors:</text>
 <paragraph id="H36CD3D2D9E544CB6A6BED786EDADB9C7"><enum>(1)</enum><text>The marketing, advertising, and labeling of the substance.</text> </paragraph><paragraph id="HB0A4A8A8A72143E88C9829B6B437860D"><enum>(2)</enum><text>The known efficacy or usefulness of the substance for the marketed, advertised or labeled purpose.</text>
 </paragraph><paragraph id="HED031AEBF3974916AC97230F3D2A7DC3"><enum>(3)</enum><text>The difference between the price at which the substance is sold and the price at which the substance it is purported to be or advertised as is normally sold.</text>
 </paragraph><paragraph id="HF469C2801C884A2DA6A2FD0B470F963A"><enum>(4)</enum><text>The diversion of the substance from legitimate channels and the clandestine importation, manufacture, or distribution of the substance.</text>
 </paragraph><paragraph id="H9476D2B4CCB94019A50CE736C74CA040"><enum>(5)</enum><text>Whether the defendant knew or should have known the substance was intended to be consumed by injection, inhalation, ingestion, or any other immediate means.</text>
 </paragraph><paragraph id="H3A97B34AB651400EBA0B17A31A6BFF58"><enum>(6)</enum><text display-inline="yes-display-inline">Any controlled substance analogue that is manufactured, formulated, sold, distributed, or marketed with the intent to avoid the provisions of existing drug laws.</text>
 </paragraph></subsection><subsection commented="no" display-inline="no-display-inline" id="H7DF0A44EBA0747448C8EBB4E6FE0B911"><enum>(c)</enum><header>Limitation</header><text>For purposes of this section, evidence that a substance was not marketed, advertised, or labeled for human consumption, by itself, shall not be sufficient to establish that the substance was not intended for human consumption.</text></subsection><after-quoted-block>.</after-quoted-block></quoted-block>
			</paragraph></section></legis-body></bill>


