# FDA recall D-0514-2019

> **ACP Nimble Buyer, Inc.** · Class III · drug recall initiated 2019-02-07.

## 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

## Reason for recall

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

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-0514-2019
- **Recalling firm:** ACP Nimble Buyer, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-02-07
- **Report date:** 2019-02-27
- **Termination date:** 2020-03-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** South Plainfield, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0514-2019

## Citation

> AI Analytics. FDA recall D-0514-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0514-2019. Source: US FDA. Licensed CC0.

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