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US law
Federal (United States)
Regulations
Title 21 CFR — Food and Drugs
Chapter I — FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Part 332 — ANTIFLATULENT PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
Subpart C — Labeling
Federal (United States) · Regulations
Subpart C — Labeling
2 sections
2 sections
21 C.F.R. § 332.30
Labeling of antiflatulent drug products.
21 C.F.R. § 332.31
Professional labeling.
Subpart C — Labeling | Federal (United States) Regulations | Justis AI