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FDAFDA · Food and drugs·Recall number D-524-2013

BroveX PSE, Antihistamine, Nasal Decongestant, 100 count bottle, OTC, Manufactured for: Pernix Therapeutics, Gonzales, LA 70737 NDC 58605-440-01

Published June 12, 2013 · Recall initiated: January 30, 2013

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

CGMP Deviations: Products are underdosed or have an incorrect dosage regime.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
TG United, Inc.
Distributor
FL, MS, SC, LA and TX
Lot
Lot# 11A001 Exp. 12/12; Lot# 11L002 Exp. 10/13; Lot # 12K007 Exp. 09/14.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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