Title 21 › Chapter CHAPTER 9— - FEDERAL FOOD, DRUG, AND COSMETIC ACT › Subchapter SUBCHAPTER VII— - GENERAL AUTHORITY › Part Part F— - National Uniformity for Nonprescription Drugs and Preemption for Labeling or Packaging of Cosmetics › § 379s
States and local governments may not make or keep rules for cosmetic labels or packaging that differ from the federal rules under this chapter, the Poison Prevention Packaging Act of 1970 (15 U.S.C. 1471 et seq.), or the Fair Packaging and Labeling Act (15 U.S.C. 1451 et seq.), except as allowed below. The federal Secretary can permit a state rule if the state asks, after notice and chance to comment, and if the rule protects an important public interest, does not conflict with federal law, and does not unduly burden interstate commerce. “State requirement” here means any specific rule about the same labeling or packaging issue, including public information or other communications. This does not change state product liability law. It also does not apply to state rules adopted by initiative or referendum before September 1, 1997.
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Food and Drugs — Source: USLM XML via OLRC
Legislative History
Reference
Citation
21 U.S.C. § 379s
Title 21 — Food and Drugs
Last Updated
Apr 6, 2026
Release point: 119-73