Citation

Fed. Regist. 1999; 64(51): 13254-13303.

Copyright

(Copyright © 1999, U.S. Office of the Federal Register, National Archives and Records Service, General Services Administration)

DOI

unavailable

PMID

10557606

Abstract

The Food and Drug Administration (FDA) is issuing a final rule establishing a standardized format and standardized content requirements for the labeling of over-the-counter (OTC) drug products. This final rule is intended to assist consumers in reading and understanding OTC drug product labeling so that consumers may use these products safely and effectively. This final rule will require all OTC drug products to carry the new, easy-to-read format and the revised content requirements within prescribed implementation periods.

Language: en