Class II · Moderate risk
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CGMP Deviations: Product was released to market prior to microbiological testing.
National Drug Code
Is NDC 11084-0010-27 recalled?
Refresh AntiBac FOAM
Yes — this exact package was recalled
1 FDA recall names the code 11084-0010-27 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 .13 g/L
- Form
- Soap · Topical
- Labeler
- SC Johnson Professional USA Inc.
- Type
- Human OTC Drug
- Product code
- 11084-0010
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.
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.