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Antibacterial Lidocaine Wound Gel

NDC 51142-652 · ASO LLC

Generic namebenzalkonium chloride, lidocaine hydrochloride
Dosage formGEL
RouteTOPICAL
Active ingredient(s)LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE
Strength.13; 2 g/100mL; g/100mL
Pharmacologic classAmide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

51142-652-14 — 1 TUBE in 1 CARTON (51142-652-14) / 14 mL in 1 TUBE

51142-652-28 — 1 TUBE in 1 CARTON (51142-652-28) / 28 mL in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50814-059 — BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE, 50814-079 — BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE, 50814-081 — BENZALKONIUM CHLORIDE, 50865-017 — E2 SANITIZING HAND, 50865-213 — benzalkonium chloride, 50865-215 — Benzalkonium chloride, 50865-683 — benzalkonium chloride, 50980-207 — Benzalkonium Chloride, 51004-2105 — Lidocaine Hydrochloride and Epinephrine Bitartrate, 51042-001 — Benzalkonium Chloride, 51209-014 — BENZALKONIUM CHLORIDE, 51209-015 — BENZALKONIUM CHLORIDE, 51209-016 — BENZALKONIUM CHLORIDE, 51209-017 — BENZALKONIUM CHLORIDE, 51209-018 — BENZALKONIUM CHLORIDE, 51209-020 — BENZALKONIUM CHLORIDE, 51209-021 — BENZALKONIUM CHLORIDE, 51209-022 — BENZALKONIUM CHLORIDE, 51209-030 — BENZALKONIUM CHLORIDE, 51209-031 — BENZALKONIUM CHLORIDE, +1808 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.