[Federal Register Volume 64, Number 72 (Thursday, April 15, 1999)]
[Rules and Regulations]
[Page 18571]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-9520]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Parts 201, 330, 331, 341, 346, 355, 358, 369, and 701

[Docket Nos. 98N-0337, 96N-0420, 95N-0259, and 90P-0201]

RIN 0910-AA79


Over-The-Counter Human Drugs; Labeling Requirements; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Final rule; correction.

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SUMMARY: The Food and Drug Administration (FDA) is correcting a final 
rule that appeared in the Federal Register of March 17, 1999 (64 FR 
13254). The final rule established a standardized format and 
standardized content requirements for the labeling of over-the-counter 
(OTC) drug products. The document was inadvertently published with an 
incorrect effective date. This document corrects that error.

DATES: Effective April 15, 1999, the effective date of the final rule 
published on March 17, 1999 (64 FR 13254) is corrected to May 16, 1999.

FOR FURTHER INFORMATION CONTACT: Debra L. Bowen, Food and Drug 
Administration, Center for Drug Evaluation and Research (HFD-560), 5600 
Fishers Lane, Rockville, MD 20852, 301-827-2222, or email 
``[email protected]''.

SUPPLEMENTARY INFORMATION: In FR Doc. 99-6296, appearing on page 13254 
in the Federal Register of Wednesday, March 17, 1999, the following 
correction is made:
     1. On page 13254, in the first column, under the ``Dates'' section 
``Effective Date: April 16, 1999.'' is corrected to read ``Effective 
Date: May 16, 1999.''

    Dated: April 12, 1999.
William K. Hubbard,
Acting Deputy Commissioner for Policy.
[FR Doc. 99-9520 Filed 4-14-99; 8:45 am]
BILLING CODE 4160-01-F