US Drug Recall Register
Class III · Low risk Terminated Initiated Feb 7, 2019 (8 years ago)

Mometasone Furoate Cream, 0.1%, 45 g tube, Rx Only, Manufactured by: G&W Laboratories…

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

Why it was recalled

Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has an NDC typographical error.

What was recalled

Mometasone Furoate Cream, 0.1%, 45 g tube, Rx Only, Manufactured by: G&W Laboratories, Inc. South Plainfield, NJ 07080, NDC 0713-0726-37

Recalling firm
ACP Nimble Buyer, Inc.
NDC code
0713-0726-37
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0514-2019

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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