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Cold, Cough, Allergy, Bronchodilator, and Antiasthmatic Drug Products for Over-the-Counter Human Use; Amendment of Monograph for OTC Nasal Decongestant Drug Products

other · Food and Drug Administration · Rule · Published 2006-08-01 · Effective 2006-08-31 · 71 FR 43358

Document

Document number
E6-12265
Federal Register citation
71 FR 43358
CFR reference
21 CFR 341
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2006-08-01
Effective date
2006-08-31
HHS docket
Docket No. 1976N-0052N

Abstract

The Food and Drug Administration (FDA) is issuing a final rule to amend the final monograph (FM) for over-the-counter (OTC) nasal decongestant drug products (drug products used to relieve nasal congestion due to a cold, hay fever, or other upper respiratory allergies) to add phenylephrine bitartrate (PEB), both individually and in combination drug products in an effervescent dosage form, as generally recognized as safe and effective (GRASE). An effervescent dosage form is intended to be dissolved in water before taking by mouth. This final rule is part of FDA's ongoing review of OTC drug products.

Source

Authoritative
Federal Register document
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