21 U.S.C. § 353c | Prereview of television advertisements

(a)

In general

The Secretary may require the submission of any television advertisement for a drug (including any script, story board, rough, or a completed video production of the television advertisement) to the Secretary for review under this section not later than 45 days before dissemination of the television advertisement.

(b)

Review

In conducting a review of a television advertisement under this section, the Secretary may make recommendations with respect to information included in the label of the drug—

(1)

on changes that are—

(A)

necessary to protect the consumer good and well-being; or

(B)

consistent with prescribing information for the product under review; and

(2)

if appropriate and if information exists, on statements for inclusion in the advertisement to address the specific efficacy of the drug as it relates to specific population groups, including elderly populations, children, and racial and ethnic minorities.

(c)

No authority to require changes

Except as provided by subsection (e), this section does not authorize the Secretary to make or direct changes in any material submitted pursuant to subsection (a).

(d)

Elderly populations, children, racially and ethnically diverse communities

In formulating recommendations under subsection (b), the Secretary shall take into consideration the impact of the advertised drug on elderly populations, children, and racially and ethnically diverse communities.

(e)

Specific disclosures

(1)

Serious risk; safety protocol

In conducting a review of a television advertisement under this section, if the Secretary determines that the advertisement would be false or misleading without a specific disclosure about a serious risk listed in the labeling of the drug involved, the Secretary may require inclusion of such disclosure in the advertisement.

(2)

Date of approval

section 355 of this title section 262 of title 42In conducting a review of a television advertisement under this section, the Secretary may require the advertisement to include, for a period not to exceed 2 years from the date of the approval of the drug under or , a specific disclosure of such date of approval if the Secretary determines that the advertisement would otherwise be false or misleading.

(f)

Rule of construction

section 352(n) of this titleNothing in this section may be construed as having any effect on requirements under or on the authority of the Secretary under section 314.550, 314.640, 601.45, or 601.94 of title 21, Code of Federal Regulations (or successor regulations).

June 25, 1938, ch. 675, § 503C Pub. L. 110–85, title IX, § 901(d)(2)Sept. 27, 2007121 Stat. 939 Pub. L. 113–54, title I, § 102(a)(1)Nov. 27, 2013127 Stat. 587(, formerly § 503B, as added , , , renumbered § 503C, , , .)

Editorial Notes

Codification

section 353b of this title Pub. L. 113–54Section was formerly classified to prior to renumbering by .

Statutory Notes and Related Subsidiaries

Effective Date

Sept. 27, 2007section 909 of Pub. L. 110–85 section 331 of this titleSection effective 180 days after , see , set out as an Effective Date of 2007 Amendment note under .