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

Is NDC 63736-0378-02 recalled?

Americaine · 57 g in 1 CAN (63736-378-02)

Yes — this exact package was recalled

1 FDA recall names the code 63736-0378-02 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
Benzocaine
Strength
BENZOCAINE 11.4 g/57g
Form
Aerosol, Spray · Topical
Labeler
Insight Pharmaceuticals LLC
Type
Human OTC Drug
Product code
63736-0378

Recalls naming this package

Class I ยท High risk

Americaine

Chemical Contamination: presence of benzene

Completed Chemical / undeclared Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company NDC 63736-378-02 D-0236-2024

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