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

Class I - Dangerous
💊 Drugs Recalled: February 7, 2019 ACP Nimble Buyer Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot #: 1009431, 1009507, Exp. 08/2020; 1009886, Exp. 09/2020
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
ACP Nimble Buyer, Inc.
Reason for Recall:
Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has an NDC typographical error.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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

Product Codes/Lot Numbers:

Lot #: 1009431, 1009507, Exp. 08/2020; 1009886, Exp. 09/2020

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0514-2019