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
The Secretary must publish draft guidance within 1 year after November 26, 2014, explaining how to follow the sunscreen rules.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
Food and Drugs — Source: USLM XML via OLRC
Legislative History
Reference
Citation
21 U.S.C. § 360fff–4
Title 21 — Food and Drugs
Last Updated
Apr 6, 2026
Release point: 119-73