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  1. US law
  2. Federal (United States)
  3. Regulations
  4. Title 21 CFR — Food and Drugs
  5. Chapter I — FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  6. Part 338 — NIGHTTIME SLEEP-AID DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
  7. Subpart C — Labeling

Federal (United States) · Regulations

Subpart C — Labeling

1 section

1 section

  • 21 C.F.R. § 338.50Labeling of nighttime sleep-aid drug products.
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