Zeasorb AF — Class III drug recall D-0142-2017
Terminated recall by GSK Consumer Healthcare, reported 2016-11-23, distributed nationwide. Labeling Not Elsewhere Classified: front labels have the incorrect NDC or 0145-1506-01 instead of the correct
| Recall number | D-0142-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GSK Consumer Healthcare, Warren, NJ, United States |
| Recall initiated | 2016-10-18 |
| Classified | 2016-11-17 |
| Reported by FDA | 2016-11-23 |
| Terminated | 2018-11-08 |
| Distributed | Nationwide (US) |
| Quantity | 462,732 bottles |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00073462150651 |
| NDC | 00145-1506-01 |
| Lot numbers | 02/18, 10/17, 11/17, 5M02ST, 5M03ST, 5M04ST, 5P01ST, 5P01STA, 5P02ST, 5P03ST, 5P04ST, 5P05ST, 6C03ST, 6C04ST, 6C05ST, 6C06ST, 6C07ST |
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".
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0142-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.