Requirements on Content and Format of Labeling for Human Prescription Drug and Biological Products

U.S. Food and Drug Administration. Requirements on Content and Format of Labeling for Human Prescription Drug and Biological Products.

Type

Web resource

Intellectual base

Web

Link

https://www.ecfr.gov/current/title-21/chapter-I/subchapter-C/part-201/subpart-B/section-201.57

Cited from

communication_media_studies

Cited by

1 citation across 1 artifact.

Each citation links to the sentence it supports in the citing article.

Primes

• Boundary Disclosure Card
  • In pharmaceuticals, package inserts carry indications, dosage, contraindications, and interactions in every box.

    This sourceFinal rule, 71 Fed. Reg. 3922 (Jan. 24, 2006). Mandates that prescription-drug labeling (package inserts) carry indications, dosage, contraindications, and interactions in a fixed order in every box.

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