Class III · Low risk
Lidocaine Wound Gel
Failed PH Specifications
National Drug Code
Is NDC 59898-0950 recalled?
Antibacterial Lidocaine Wound Gel
This product was recalled — in other package sizes
No FDA recall names your exact package code, but 1 recall cover the same product (59898-0950) in a different bottle or carton size. Worth checking with your pharmacist.
1 of these recalls is still ongoing.
- Active ingredient
- Benzalkonium Chloride, Lidocaine Hydrochloride
- Strength
- LIDOCAINE HYDROCHLORIDE 2 g/100mL; BENZALKONIUM CHLORIDE…
- Form
- Gel · Topical
- Labeler
- Water-Jel Technologies, LLC
- Type
- Human OTC Drug
- Product code
- 59898-0950
Recalls of this product
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.
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