Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 49035-0812-01 recalled?

Clotrimazole Athletes Foot · 1 TUBE in 1 CARTON (49035-812-01) / 15 g in 1 TUBE

Yes — this exact package was recalled

1 FDA recall names the code 49035-0812-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Clotrimazole
Strength
CLOTRIMAZOLE 10 mg/g
Form
Cream · Topical
Labeler
Wal-Mart Stores, Inc.
Type
Human OTC Drug
Product code
49035-0812

Recalls naming this package

Class II ยท Moderate risk

Equate Athlete's Foot

Failed Impurities/Degradation Specifications: An unknown degradation impurity was detected slightly above the specification limit in Clotrimazole Cream USP 1%.

Terminated Impurity / degradation Taro Pharmaceuticals U.S.A., Inc. NDC 49035-812-01 D-0151-2021

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler