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

Is NDC 13548-0132-03 recalled?

Acanya

Yes — this exact package was recalled

1 FDA recall names the code 13548-0132-03 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
Clindamycin Phosphate and Benzoyl Peroxide
Strength
CLINDAMYCIN PHOSPHATE 10 mg/g; BENZOYL PEROXIDE 25 mg/g
Form
Gel · Topical
Labeler
Bausch Health US, LLC
Type
Human Prescription Drug
Product code
13548-0132

Recalls naming this package

Class III ยท Low risk

Acanya (Clindamycin Phosphate and Benzoyl Peroxide)

Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being carried out due to an incorrect expiration date assigned to a lot of physicians samples.

Terminated Labeling / mix-up Valeant Pharmaceuticals North Am NDC 13548-132-03 D-020-2014

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.