IIB
110th CONGRESS
1st Session
H. R. 970
IN THE SENATE OF THE UNITED STATES
October 16, 2007
Received; read twice and referred to the Committee on Health, Education, Labor, and Pensions
AN ACT
To amend the Federal Food, Drug, and Cosmetic Act with respect to the distribution of the drug dextromethorphan, and for other purposes.
Short title
This Act may be cited as the
Dextromethorphan Distribution Act of
2007
.
Restrictions on distribution of bulk dextromethorphan
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 506D.
; and
by inserting after section 506C the following:
Restrictions on distribution of bulk dextromethorphan
Restrictions
No person shall—
possess or receive unfinished dextromethorphan, unless the person is registered under section 510; or
distribute unfinished dextromethorphan to any person other than a person registered under section 510.
Exception for common carriers
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 registered under section 510.
Definitions
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.
.
Passed the House of Representatives October 15, 2007.
Lorraine C. Miller,
Clerk