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

Is NDC 0924-0251-00 recalled?

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Yes — this exact package was recalled

1 FDA recall names the code 0924-0251-00 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.

1 of these recalls is still ongoing.

Active ingredient
Isoprpoyl Alcohol
Strength
ISOPROPYL ALCOHOL 70 mL/100mL
Form
Swab · Topical
Labeler
Acme United Corporation
Type
Human OTC Drug
Product code
0924-0251

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