Mometasone Furoate Cream recall: Labeling Error
Mometasone Furoate Cream, 0.1%, 45 g tube, Rx Only, Manufactured by: G&W Laboratories, Inc. South Plainfield, NJ 07080, NDC 0713-0726-37
Why was Mometasone Furoate Cream recalled?
Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has an NDC typographical error.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 1009431, 1009507, Exp. 08/2020; 1009886, Exp. 09/2020
- Product
- 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.
- Quantity
- 58,176 units
- Distribution
- Nationwide within the United States
- Recall date
- February 27, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)