Sec. 3. Restrictions on distribution of bulk dextromethorphan
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The Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 321 et seq. ) is amended— in section 501, by inserting at the end the following: If it is unfinished dextromethorphan and is possessed, received, or distributed in violation of section 506H. ; and by inserting after section 506F the following: No person shall— possess or receive unfinished dextromethorphan, unless the person is registered under section 510 or otherwise registered, licensed, or approved pursuant to Federal or State law to engage in the practice of pharmacy, pharmaceutical production, or manufacture or distribution of drug ingredients; or distribute unfinished dextromethorphan to any person other than a person registered under section 510 or otherwise registered, licensed, or approved pursuant to Federal or State law to engage in the practice of pharmacy, pharmaceutical production, or manufacture or distribution of drug ingredients.
This section does not apply to a common carrier that possesses, receives, or distributes unfinished dextromethorphan for purposes of distributing such unfinished dextromethorphan between persons described in subsection
(a)as registered, licensed, or approved. In this section: The term common carrier means any person that holds itself out to the general public as a provider for hire of the transportation by water, land, or air of merchandise, whether or not the person actually operates the vessel, vehicle, or aircraft by which the transportation is provided, between a port or place and a port or place in the United States. The term unfinished dextromethorphan means dextromethorphan that is not contained in a drug that is in finished dosage form. ; and by amending section 303, as amended by section 2(b), by adding at the end the following: Notwithstanding subsection (a), a person who violates section 506H shall be subject to a civil penalty of not more than $100,000. .
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Sec. 3
Restrictions on distribution of bulk dextromethorphan
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