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

Is NDC 10223-0202-04 recalled?

Cetacaine Anesthetic

Yes — this exact package was recalled

1 FDA recall names the code 10223-0202-04 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, Butamben, and Tetracaine Hydrochloride
Strength
BENZOCAINE .028 g/.2g; BUTAMBEN .004 g/.2g; TETRACAINE…
Form
Solution · Topical
Labeler
Cetylite Industries, Inc.
Type
Human Prescription Drug
Product code
10223-0202

Recalls naming this package

Class II · Moderate risk

Cetacaine Liquid Topical Anesthetic

Subpotent Drug: Cetacaine Topical Anesthetic Liquid is being recalled because one of the three active ingredients, tetracaine, is below the specification limit at the 21 month stability test point.

Terminated Wrong potency / content Cetylite Industries, Inc. NDC 10223-0202-2 D-019-2014

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.