Sample Drug Regulation Act

Sample Drug Regulation Act - Deems a sample prescription drug to be misbranded, under the Federal Food, Drug, and Cosmetic Act, if at any time its label fails to bear the statement "Sample Drug" or if any dispenser charges a price or fee for such drug. Limits the distribution of sample drugs. Requires persons legally engaged in manufacturing, compounding, processing, distributing, or dispensing drugs for introduction into interstate commerce to maintain accurate records which shall be accessible to investigation by the Secretary of Health, Education, and Welfare.