Class III · Low risk
Dermoplast FIRST AID ANTIBACTERIAL SPRAY
Subpotent Drug: Low assay observed in one of the two active ingredients during stability testing.
National Drug Code
Is NDC 16864-0670-01 recalled?
Dermoplast First Aid · 78 g in 1 CAN (16864-670-01)
Yes — this exact package was recalled
1 FDA recall names the code 16864-0670-01 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
- BENZETHONIUM CHLORIDE and BENZOCAINE
- Strength
- BENZETHONIUM CHLORIDE 2 mg/g; BENZOCAINE 200 mg/g
- Form
- Spray · Topical
- Labeler
- Advantice Health, LLC
- Type
- Human OTC Drug
- Product code
- 16864-0670
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
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