US Drug Recall Register
Class III · Low risk Terminated Initiated Sep 20, 2012 (14 years ago)

Children's Cetirizine HCl Chewable Tablets 5 mg, 30 count blister pack, Manufactured in…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Impurity/Degradation; exceeded impurity specification at the 8 and 15 month time points (betacyclodextrin ester 1&2)

What was recalled

Children's Cetirizine HCl Chewable Tablets 5 mg, 30 count blister pack, Manufactured in India by Sandoz Private Ltd., for Sandoz Inc., Princeton, NJ NDC 0781-5283-64 --- ALSO sold under Major brand All Day Allergy Children's Cetirizine HCl 5 mg, 5 count blister pack, Major Pharmaceuticals, Livonia, MI NDC 0904-5878-33

Recalling firm
Sandoz Incorporated
NDC code
0781-5283-64
Origin
CO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-008-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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