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

Is NDC 76402-0403-03 recalled?

Hillyard Alcohol Free Foaming Instant Hand Sanitizer · 1250 mL in 1 BOTTLE, PLASTIC (76402-403-03)

Yes — this exact package was recalled

1 FDA recall names the code 76402-0403-03 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
Benzalkonium Chloride
Strength
BENZALKONIUM CHLORIDE .1 g/100mL
Form
Liquid · Topical
Labeler
Hillyard GMP
Type
Human OTC Drug
Product code
76402-0403

Recalls naming this package

Class II ยท Moderate risk

Hillyard

Microbial Contamination of Non-Sterile Products: The product may be contaminated with bacteria.

Terminated Microbial contamination Hillyard GMP NDC 76402-403-03 D-140-2013

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.