Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Mometasone Furoate Cream Recalled by ACP Nimble Buyer, Inc. Due to Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has...

Date: February 7, 2019
Company: ACP Nimble Buyer, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact ACP Nimble Buyer, Inc. directly.

Affected Products

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

Quantity: 58,176 units

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About ACP Nimble Buyer, Inc.

ACP Nimble Buyer, Inc. has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report