Citation

Fed. Regist. 2000; 65(1): 7-9.

Copyright

(Copyright © 2000, U.S. Office of the Federal Register, National Archives and Records Service, General Services Administration)

DOI

unavailable

PMID

11010625

Abstract

The Food and Drug Administration (FDA) is amending the regulation that established a standardized format and standardized content requirements for the labeling of over-the-counter (OTC) drug products, and is amending several related OTC drug product labeling regulations. This amendment corrects and conforms several aspects of the new labeling requirements to other regulatory provisions and eliminates unnecessary text from the new labeling regulation.

Language: en