Title 21Food and DrugsRelease 119-73

§360fff–4 Guidance; other provisions

Title 21 › Chapter CHAPTER 9— - FEDERAL FOOD, DRUG, AND COSMETIC ACT › Subchapter SUBCHAPTER V— - DRUGS AND DEVICES › Part Part I— - Nonprescription Sunscreen and Other Active Ingredients › § 360fff–4

Last updated Apr 6, 2026|Official source

Summary

The Secretary must publish draft guidance within 1 year after November 26, 2014, explaining how to follow the sunscreen rules. The draft must cover what to include in sponsor submissions, what data prove a nonprescription sunscreen ingredient is safe and works, how a sponsor can withdraw a request, and how the Secretary will handle all requests and pending requests. The Secretary must finalize that guidance within 2 years after November 26, 2014. Chapter 35 of title 44 does not apply to information collected for that guidance. People may begin sending submissions on November 26, 2014, and the Secretary must review and act on them. The rule does not change how sunscreens already sold across state lines on November 26, 2014 are marketed, except as this part says. The Secretary still may stop or restrict marketing of sunscreens that are not safe, effective, or are misbranded. The Secretary’s authority over other drugs and over drugs approved under section 355 or section 351 of the Public Health Service Act is not changed. Timelines for certain procedures in section 360fff–3(a) (paragraphs (1), (2), (5), and (6)) do not apply to requests sent more than 6 years after November 26, 2014 (after November 26, 2020).

Full Legal Text

Title 21, §360fff–4

Food and Drugs — Source: USLM XML via OLRC

(a)(1)(A)Not later than 1 year after November 26, 2014, the Secretary shall issue draft guidance on the implementation of, and compliance with, the requirements with respect to sunscreen under this part, including guidance on—
(i)the format and content of information submitted by a sponsor in support of a request under section 360fff–1 of this title or a pending request;
(ii)the data required to meet the safety and efficacy standard for determining whether a nonprescription sunscreen active ingredient or combination of nonprescription sunscreen active ingredients is GRASE and is not misbranded;
(iii)the process by which a request under section 360fff–1 of this title or a pending request is withdrawn; and
(iv)the process by which the Secretary will carry out section 360fff–3(c) of this title, including with respect to how the Secretary will address the total number of requests received under section 360fff–1 of this title and pending requests.
(B)The Secretary shall finalize the guidance described in subparagraph (A) not later than 2 years after November 26, 2014.
(C)Chapter 35 of title 44 shall not apply to collections of information made for purposes of guidance under this subsection.
(2)Irrespective of whether final guidance under paragraph (1) has been issued—
(A)persons may, beginning on November 26, 2014, make submissions under this part; and
(B)the Secretary shall review and act upon such submissions in accordance with this part.
(b)(1)Nothing in this part shall be construed to affect the marketing of sunscreens that are marketed in interstate commerce on or before November 26, 2014, except as otherwise provided in this part.
(2)Nothing in this part shall be construed to alter the authority of the Secretary with respect to prohibiting the marketing of a sunscreen that is not safe and effective or is misbranded, or with respect to imposing restrictions on the marketing of a sunscreen to ensure safety and effectiveness, except as otherwise provided in this part, including section 360fff–3(e) of this title.
(3)Except as otherwise provided in section 360fff–6 of this title, nothing in this part shall be construed to affect the authority of the Secretary under this chapter or the Public Health Service Act (42 U.S.C. 201 et seq.) with respect to a drug other than a nonprescription sunscreen.
(4)Nothing in this part shall affect the marketing of a drug approved under section 355 of this title or section 351 of the Public Health Service Act [42 U.S.C. 262].
(c)The timelines for the processes and procedures under paragraphs (1), (2), (5), and (6) of section 360fff–3(a) of this title shall not apply to any requests submitted to the Secretary under section 360fff–1 of this title after the date that is 6 years after November 26, 2014.

Legislative History

Notes & Related Subsidiaries

Editorial Notes

References in Text

The Public Health Service Act, referred to in subsec. (b)(3), is act July 1, 1944, ch. 373, 58 Stat. 682, which is classified generally to chapter 6A (§ 201 et seq.) of Title 42, The Public Health and Welfare. For complete classification of this Act to the Code, see

Short Title

note set out under section 201 of Title 42 and Tables.

Reference

Citations & Metadata

Citation

21 U.S.C. § 360fff–4

Title 21Food and Drugs

Last Updated

Apr 6, 2026

Release point: 119-73