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

Is NDC 50227-1002-03 recalled?

Patterson Dental Topical Anesthetic · 30 g in 1 JAR (50227-1002-3)

Yes — this exact package was recalled

1 FDA recall names the code 50227-1002-03 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
Benzocaine
Strength
BENZOCAINE 200 mg/g
Form
Gel · Dental
Labeler
Patterson Dental
Type
Human OTC Drug
Product code
50227-1002

Recalls naming this package

Class II · Moderate risk

Patterson Dental

CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.

Terminated cGMP deviation Keystone Industries NDC 50227-1002-3 D-0141-2025

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