II 112th CONGRESS 2d Session S. 3376 IN THE SENATE OF THE UNITED STATES July 11, 2012 Mr. Casey (for himself and Ms. Murkowski) introduced the following bill; which was read twice and referred to the Committee on Health, Education, Labor, and Pensions A BILL To amend the Federal Food, Drug, and Cosmetic Act to prevent the abuse of dextromethorphan, and for other purposes.

1.

Short title

This Act may be cited as the Preventing Abuse of Cough Treatments Act of 2012 or the PACT Act.

2.

Sales of over-the-counter drugs containing dextromethorphan

(a)

Prohibited act

Section 301 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 331) is amended by adding at the end the following: (aaa)(1)(A)Except as provided in subparagraph (2), the sale or offering for sale of a drug containing dextromethorphan to an individual under 18 years of age, including any such sale using the Internet, provided the drug is not subject to section 503(b)(1). (B)If a person fails to request identification from an individual under 18 years of age and sells a product containing dextromethorphan to that individual, that person shall be deemed to have known that the individual was under 18 years of age. (C)It shall be an affirmative defense to an alleged violation of clause (A) that the person selling a product containing dextromethorphan examined the purchaser's identification card and, based on that examination, that person reasonably concluded that the identification was valid and indicated that the purchaser was not less than 18 years of age. (2)(A)This paragraph shall not apply to any sale made pursuant to a validly issued prescription. (B)This paragraph shall not apply to the sale or offering for sale of a drug containing dextromethorphan to an individual under 18 years of age if such individual supplies proof at the time of such sale that such individual— (i)is married; (ii)is the parent of a child; or (iii)is actively enrolled in the military. (3)In this paragraph, the term identification card mean an identification card that— (A)includes a photograph and the date of birth of the individual; and (B)is issued by a State or the Federal Government or is considered acceptable for purposes of sections 274a.2(b)(1)(v)(A) and 274a.2(b)(1)(v)(B)(1) of title 8, Code of Federal Regulations (as in effect on or after the date of the enactment of the Preventing Abuse of Cough Treatments Act of 2012). . (b)

Civil penalties

Section 303 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 333) is amended by adding at the end the following: (h)(1)Notwithstanding subsection (a), a person who violates section 301(aaa) shall be subject to a civil penalty in an amount— (A)not more than $1,000 for the first such violation by a person; (B)not more than $2,000 for the second such violation by a person; and (C)not more than $5,000 for the third such violation, or a subsequent such violation, by a person. (2)In determining the amount of a civil penalty under this subsection for a person who is a retailer, the Secretary shall consider whether the retailer has taken appropriate steps to prevent subsequent violations, such as— (A)the establishment and administration of a documented employee training program to ensure all employees are familiar with and abiding by the provisions of this section; or (B)other actions taken by a retailer to ensure compliance with this section. (3)If a person who is a retailer transacts sales of products containing dextromethorphan at more than one physical location, for purposes of determining the number of violations by that person under this subsection, each individual physical location operated by that retailer shall be considered a separate person. (4)In this subsection, the term retailer means a grocery store, general merchandise store, drug store, pharmacy, convenience store, or other entity or person whose activities as a distributor relating to products containing dextromethorphan are limited almost exclusively to sales for personal use, both in number of sales and volume of sales, either directly to walk-in customers or in face-to-face transactions by direct sales. .

3.

Restrictions on distribution of bulk dextromethorphan

The Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321 et seq.) is amended— (1)in section 501, by inserting at the end the following: (j)If it is unfinished dextromethorphan and is possessed, received, or distributed in violation of section 506D. ; (2)by inserting after section 506C the following:

506D.

Restrictions on the distribution of bulk dextromethorphan

(a)

In general

No person shall— (1)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 (2)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. (b)

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 described in subsection (a) as registered, licensed, or approved. (c)

Definitions

In this section: (1)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. (2)The term unfinished dextromethorphan means dextromethorphan that is not contained in a drug that is in finished dosage form.

; and (3)by amending section 303, as amended by section 2(b), by adding at the end the following: (i)Notwithstanding subsection (a), a person who violates section 506D shall be subject to a civil penalty of not more than $100,000. .