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

Is NDC 0713-0656-31 recalled?

Clobetasol Propionate · 1 TUBE in 1 CARTON (0713-0656-31) / 30 g in 1 TUBE

Yes — this exact package was recalled

1 FDA recall names the code 0713-0656-31 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
Clobetasol Propionate
Strength
CLOBETASOL PROPIONATE .5 mg/g
Form
Ointment · Topical
Labeler
Cosette Pharmaceuticals, Inc.
Type
Human Prescription Drug
Product code
0713-0656

Recalls naming this package

Class III · Low risk

G & W Clobetasol Propionate Ointment 0.05%

Failed impurities/degradation specifications: This product is being recalled due to out of specification results for Clobetasol Related Compound A, a known impurity which is a degradation product.

Terminated Impurity / degradation G & W Laboratories, Inc. NDC 0713-0656-15 D-0945-2017

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