[Federal Register Volume 59, Number 135 (Friday, July 15, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-17150]


[[Page Unknown]]

[Federal Register: July 15, 1994]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 341

[Docket No. 89P-0040]
RIN 0905-AA06

 

Cold, Cough, Allergy, Bronchodilator, and Antiasthmatic Drug 
Products for Over-The-Counter Human Use; Amendment of Final Monograph 
for OTC Antitussive Drug Products; 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 June 3, 1994 (59 FR 
29172). The document amended the final monograph for over-the-counter 
(OTC) antitussive drug products to include the ingredients 
diphenhydramine citrate and diphenhydramine hydrochloride. The document 
was published with some errors. This document corrects those errors.

EFFECTIVE DATE: June 5, 1995.

FOR FURTHER INFORMATION CONTACT: William E. Gilbertson, Center for Drug 
Evaluation and Research (HFD-810), Food and Drug Administration, 5600 
Fishers Lane, Rockville, MD 20857, 301-594-5000.

    In FR Doc. 94-13586, appearing on page 29172 in the Federal 
Register of Friday, June 3, 1994, the following corrections are made:


Sec. 341.74  [Corrected]

    1. On page 29174, in the third column, in Sec. 341.74 Labeling of 
antitussive drug products, paragraphs (d)(1)(iv) and (d)(1)(v) are 
corrected by removing the quotation marks.


Sec. 341.90  [Corrected]

    2. On page 29174, in the third column, in Sec. 341.90 Professional 
labeling, paragraphs (r) and (s) are corrected by removing the 
quotation marks.

    Dated: July 8, 1994.
Michael R. Taylor,
Deputy Commissioner for Policy.
[FR Doc. 94-17150 Filed 7-14-94; 8:45 am]
BILLING CODE 4160-01-F