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

Is NDC 64009-0333-95 recalled?

Lite nFoamy E2 Sanitizing Handwash · 3.79 L in 1 CONTAINER (64009-333-95)

Yes — this exact package was recalled

1 FDA recall names the code 64009-0333-95 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 1.3 g/L
Form
Soap · Topical
Labeler
Spartan Chemical Company, Inc.
Type
Human OTC Drug
Product code
64009-0333

Recalls naming this package

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