Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Zeasorb AF (miconazole nitrate) Recalled by GSK Consumer Healthcare Due to Labeling Not Elsewhere Classified: front labels have the...
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 GSK Consumer Healthcare directly.
Affected Products
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
Quantity: 462,732 bottles
Why Was This Recalled?
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".
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GSK Consumer Healthcare
GSK Consumer Healthcare has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report