# FDA recall D-0142-2017

> **GSK Consumer Healthcare** · Class III · drug recall initiated 2016-10-18.

## Product

Zeasorb AF (miconazole nitrate), 2%, cures most athlete's foot, Net wt. 2.5 OZ (71 g), Manufactured for: Steifel Laboratories, Inc., Research Triangle Park, NC 27709, UPC 0 73462 15065 1; NDC 0145-1506-01

## Reason for recall

Labeling Not Elsewhere Classified: front labels have the incorrect NDC or 0145-1506-01 instead of the correct NDC of 0145-1506-05 and some back labels have the incorrect indication stating "use for the cure of most jock itch" rather than "use for the cure of most athlete's foot".

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0142-2017
- **Recalling firm:** GSK Consumer Healthcare
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-10-18
- **Report date:** 2016-11-23
- **Termination date:** 2018-11-08

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0142-2017

## Citation

> AI Analytics. FDA recall D-0142-2017. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0142-2017. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*