21 USC 387j - Application for review of certain tobacco products

U.S Code last checked for updates: Nov 22, 2024

§ 387j.

Application for review of certain tobacco products

(a)

In general

(1)

New tobacco product defined

For purposes of this section the term “new tobacco product” means—

(A)

any tobacco product (including those products in test markets) that was not commercially marketed in the United States as of February 15, 2007; or

(B)

any modification (including a change in design, any component, any part, or any constituent, including a smoke constituent, or in the content, delivery or form of nicotine, or any other additive or ingredient) of a tobacco product where the modified product was commercially marketed in the United States after February 15, 2007.

(2)

Premarket review required

(A)

New products

An order under subsection (c)(1)(A)(i) for a new tobacco product is required unless—

(i)

the manufacturer has submitted a report under section 387e(j) of this title; and the Secretary has issued an order that the tobacco product—

(I)

is substantially equivalent to a tobacco product commercially marketed (other than for test marketing) in the United States as of February 15, 2007; and

(II)

is in compliance with the requirements of this chapter; or

(ii)

the tobacco product is exempt from the requirements of section 387e(j) of this title pursuant to a regulation issued under section 387e(j)(3) of this title.

(B)

Application to certain post-February 15, 2007, products

Subparagraph (A) shall not apply to a tobacco product—

(i)

that was first introduced or delivered for introduction into interstate commerce for commercial distribution in the United States after February 15, 2007, and prior to the date that is 21 months after June 22, 2009; and

(ii)

for which a report was submitted under section 387e(j) of this title within such 21-month period,

except that subparagraph (A) shall apply to the tobacco product if the Secretary issues an order that the tobacco product is not substantially equivalent.

(3)

Substantially equivalent defined

(A)

In general

In this section and section 387e(j) of this title, the term “substantially equivalent” or “substantial equivalence” means, with respect to the tobacco product being compared to the predicate tobacco product, that the Secretary by order has found that the tobacco product—

(i)

has the same characteristics as the predicate tobacco product; or

(ii)

has different characteristics and the information submitted contains information, including clinical data if deemed necessary by the Secretary, that demonstrates that it is not appropriate to regulate the product under this section because the product does not raise different questions of public health.

(B)

Characteristics

(C)

Limitation

(4)

Health information

(A)

Summary

(B)

Required information

(b)

Application

(1)

Contents

An application under this section shall contain—

(A)

full reports of all information, published or known to, or which should reasonably be known to, the applicant, concerning investigations which have been made to show the health risks of such tobacco product and whether such tobacco product presents less risk than other tobacco products;

(B)

a full statement of the components, ingredients, additives, and properties, and of the principle or principles of operation, of such tobacco product;

(C)

a full description of the methods used in, and the facilities and controls used for, the manufacture, processing, and, when relevant, packing and installation of, such tobacco product;

(D)

an identifying reference to any tobacco product standard under section 387g of this title which would be applicable to any aspect of such tobacco product, and either adequate information to show that such aspect of such tobacco product fully meets such tobacco product standard or adequate information to justify any deviation from such standard;

(E)

such samples of such tobacco product and of components thereof as the Secretary may reasonably require;

(F)

specimens of the labeling proposed to be used for such tobacco product; and

(G)

such other information relevant to the subject matter of the application as the Secretary may require.

(2)

Referral to Tobacco Products Scientific Advisory Committee

Upon receipt of an application meeting the requirements set forth in paragraph (1), the Secretary—

(A)

may, on the Secretary’s own initiative; or

(B)

may, upon the request of an applicant,

refer such application to the Tobacco Products Scientific Advisory Committee for reference and for submission (within such period as the Secretary may establish) of a report and recommendation respecting the application, together with all underlying data and the reasons or basis for the recommendation.

(c)

Action on application

(1)

Deadline

(A)

In general

As promptly as possible, but in no event later than 180 days after the receipt of an application under subsection (b), the Secretary, after considering the report and recommendation submitted under subsection (b)(2), shall—

(i)

issue an order that the new product may be introduced or delivered for introduction into interstate commerce if the Secretary finds that none of the grounds specified in paragraph (2) of this subsection applies; or

(ii)

issue an order that the new product may not be introduced or delivered for introduction into interstate commerce if the Secretary finds (and sets forth the basis for such finding as part of or accompanying such denial) that 1 or more grounds for denial specified in paragraph (2) of this subsection apply.

(B)

Restrictions on sale and distribution

(2)

Denial of application

The Secretary shall deny an application submitted under subsection (b) if, upon the basis of the information submitted to the Secretary as part of the application and any other information before the Secretary with respect to such tobacco product, the Secretary finds that—

(A)

there is a lack of a showing that permitting such tobacco product to be marketed would be appropriate for the protection of the public health;

(B)

the methods used in, or the facilities or controls used for, the manufacture, processing, or packing of such tobacco product do not conform to the requirements of section 387f(e) of this title;

(C)

based on a fair evaluation of all material facts, the proposed labeling is false or misleading in any particular; or

(D)

such tobacco product is not shown to conform in all respects to a tobacco product standard in effect under section 387g of this title, and there is a lack of adequate information to justify the deviation from such standard.

(3)

Denial information

(4)

Basis for finding

For purposes of this section, the finding as to whether the marketing of a tobacco product for which an application has been submitted is appropriate for the protection of the public health shall be determined with respect to the risks and benefits to the population as a whole, including users and nonusers of the tobacco product, and taking into account—

(A)

the increased or decreased likelihood that existing users of tobacco products will stop using such products; and

(B)

the increased or decreased likelihood that those who do not use tobacco products will start using such products.

(5)

Basis for action

(A)

Investigations

(B)

Other evidence

(d)

Withdrawal and temporary suspension

(1)

In general

The Secretary shall, upon obtaining, where appropriate, advice on scientific matters from the Tobacco Products Scientific Advisory Committee, and after due notice and opportunity for informal hearing for a tobacco product for which an order was issued under subsection (c)(1)(A)(i), issue an order withdrawing the order if the Secretary finds—

(A)

that the continued marketing of such tobacco product no longer is appropriate for the protection of the public health;

(B)

that the application contained or was accompanied by an untrue statement of a material fact;

(C)

that the applicant—

(i)

has failed to establish a system for maintaining records, or has repeatedly or deliberately failed to maintain records or to make reports, required by an applicable regulation under section 387i of this title;

(ii)

has refused to permit access to, or copying or verification of, such records as required by section 374 of this title; or

(iii)

has not complied with the requirements of section 387e of this title;

(D)

on the basis of new information before the Secretary with respect to such tobacco product, evaluated together with the evidence before the Secretary when the application was reviewed, that the methods used in, or the facilities and controls used for, the manufacture, processing, packing, or installation of such tobacco product do not conform with the requirements of section 387f(e) of this title and were not brought into conformity with such requirements within a reasonable time after receipt of written notice from the Secretary of nonconformity;

(E)

on the basis of new information before the Secretary, evaluated together with the evidence before the Secretary when the application was reviewed, that the labeling of such tobacco product, based on a fair evaluation of all material facts, is false or misleading in any particular and was not corrected within a reasonable time after receipt of written notice from the Secretary of such fact; or

(F)

on the basis of new information before the Secretary, evaluated together with the evidence before the Secretary when such order was issued, that such tobacco product is not shown to conform in all respects to a tobacco product standard which is in effect under section 387g of this title, compliance with which was a condition to the issuance of an order relating to the application, and that there is a lack of adequate information to justify the deviation from such standard.

(2)

Appeal

(3)

Temporary suspension

(e)

Service of order

An order issued by the Secretary under this section shall be served—

(1)

in person by any officer or employee of the department designated by the Secretary; or

(2)

by mailing the order by registered mail or certified mail addressed to the applicant at the applicant’s last known address in the records of the Secretary.

(f)

Records

(1)

Additional information

(2)

Access to records

(g)

Investigational tobacco product exemption for investigational use

(June 25, 1938, ch. 675, § 910, as added Pub. L. 111–31, div. A, title I, § 101(b)(3), June 22, 2009, 123 Stat. 1807.)

cite as: 21 USC 387j