FDA Drug Recalls

Recalls / Class II

Class IID-516-2013

Product

NoHist TABLETS, Antihistamine, Nasal Decongestant, 100 count bottle, OTC, Distributed by: Larken Laboratories, Inc., Canton, MS 39046, NDC 68047-173-01

Affected lot / code info
Lot# 11K010 Exp. 09/13.

Why it was recalled

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

Recalling firm

Firm
TG United, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
16275 Aviation Loop Dr, N/A, Brooksville, Florida 34604-6805

Distribution

Quantity
4824 bottles - 100-count
Distribution pattern
FL, MS, SC, LA and TX

Timeline

Recall initiated
2013-01-30
FDA classified
2013-06-04
Posted by FDA
2013-06-12
Terminated
2016-09-30
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-516-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.