Dietary Supplement and Nonprescription Drug Consumer Protection Act

Pub. L. 109–462

US Codex doesn’t hold the enacted text of this law — the public-law corpus runs from the 113th Congress (2013) onward. What it changed in the U.S. Code, reconstructed from the credit notes, is listed below.

7 sections of the Code credited to this law, found between Public Law 109-173 and Public Law 109-482.

• 21 U.S.C. § 331 — Prohibited acts
• 21 U.S.C. § 343 — Misbranded food
• 21 U.S.C. § 352 — Misbranded drugs and devices
• 21 U.S.C. § 379aa — Serious adverse event reporting for nonprescription drugs
• 21 U.S.C. § 379aa-1 — 379aa–1. Serious adverse event reporting for dietary supplements
• 21 U.S.C. § 381 — Imports and exports
• 21 U.S.C. § 379aa–1 — Serious adverse event reporting for dietary supplements