<section xmlns="http://xml.house.gov/schemas/uslm/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" style="-uslm-lc:I80" id="id41af117a-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813"><num value="813">§ 813.</num><heading> Treatment of controlled substance analogues</heading><subsection style="-uslm-lc:I19" class="indent2 firstIndent-2" id="id41af117b-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813/a"><num value="a" class="bold">(a)</num><heading class="bold"> In general</heading><content><p style="-uslm-lc:I11" class="indent0">A controlled substance analogue shall, to the extent intended for human consumption, be treated, for the purposes of any Federal law as a controlled substance in schedule I.</p>
</content>
</subsection>
<subsection style="-uslm-lc:I19" class="indent2 firstIndent-2" id="id41af117c-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813/b"><num value="b" class="bold">(b)</num><heading class="bold"> Determination</heading><chapeau>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:</chapeau><paragraph style="-uslm-lc:I12" class="indent1" id="id41af117d-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813/b/1"><num value="1">(1)</num><content> The marketing, advertising, and labeling of the substance.</content>
</paragraph>
<paragraph style="-uslm-lc:I12" class="indent1" id="id41af117e-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813/b/2"><num value="2">(2)</num><content> The known efficacy or usefulness of the substance for the marketed, advertised, or labeled purpose.</content>
</paragraph>
<paragraph style="-uslm-lc:I12" class="indent1" id="id41af117f-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813/b/3"><num value="3">(3)</num><content> 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.</content>
</paragraph>
<paragraph style="-uslm-lc:I12" class="indent1" id="id41af1180-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813/b/4"><num value="4">(4)</num><content> The diversion of the substance from legitimate channels and the clandestine importation, manufacture, or distribution of the substance.</content>
</paragraph>
<paragraph style="-uslm-lc:I12" class="indent1" id="id41af1181-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813/b/5"><num value="5">(5)</num><content> Whether the defendant knew or should have known the substance was intended to be consumed by injection, inhalation, ingestion, or any other immediate means.</content>
</paragraph>
<paragraph style="-uslm-lc:I12" class="indent1" id="id41af1182-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813/b/6"><num value="6">(6)</num><content> Any controlled substance analogue that is manufactured, formulated, sold, distributed, or marketed with the intent to avoid the provisions of existing drug laws.</content>
</paragraph>
</subsection>
<subsection style="-uslm-lc:I19" class="indent2 firstIndent-2" id="id41af1183-a3d3-11e9-95d4-f3ff9237185e" identifier="/us/usc/t21/s813/c"><num value="c" class="bold">(c)</num><heading class="bold"> Limitation</heading><content><p style="-uslm-lc:I11" class="indent0">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.</p>
</content>
</subsection>
<sourceCredit id="id41af1184-a3d3-11e9-95d4-f3ff9237185e">(<ref href="/us/pl/91/513/tII/s203">Pub. L. 91–513, title II, § 203</ref>, as added <ref href="/us/pl/99/570/tI/s1202">Pub. L. 99–570, title I, § 1202</ref>, <date date="1986-10-27">Oct. 27, 1986</date>, <ref href="/us/stat/100/3207-13">100 Stat. 3207–13</ref>; amended <ref href="/us/pl/100/690/tVI/s6470/c">Pub. L. 100–690, title VI, § 6470(c)</ref>, <date date="1988-11-18">Nov. 18, 1988</date>, <ref href="/us/stat/102/4378">102 Stat. 4378</ref>; <ref href="/us/pl/115/271/tIII/s3241">Pub. L. 115–271, title III, § 3241</ref>, <date date="2018-10-24">Oct. 24, 2018</date>, <ref href="/us/stat/132/3950">132 Stat. 3950</ref>.)</sourceCredit>
<notes type="uscNote" id="id41af1185-a3d3-11e9-95d4-f3ff9237185e">
<note style="-uslm-lc:I75" topic="referencesInText" id="id41af1186-a3d3-11e9-95d4-f3ff9237185e">
<heading class="centered smallCaps">References in Text</heading><p style="-uslm-lc:I21" class="indent0">Schedule I, referred to in subsec. (a), is set out in <ref href="/us/usc/t21/s812/c">section 812(c) of this title</ref>.</p>
</note>
<note style="-uslm-lc:I74" topic="amendments" id="id41af1187-a3d3-11e9-95d4-f3ff9237185e"><heading class="centered smallCaps">Amendments</heading><p style="-uslm-lc:I21" class="indent0">2018—<ref href="/us/pl/115/271">Pub. L. 115–271</ref> designated existing provisions as subsec. (a), inserted heading, and added subsecs. (b) and (c).</p>
<p style="-uslm-lc:I21" class="indent0">1988—<ref href="/us/pl/100/690">Pub. L. 100–690</ref> substituted “any Federal law” for “this subchapter and subchapter II of this chapter”.</p>
</note>
</notes>
</section>