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PURELL Antimicrobial Foaming Hand

NDC 21749-610 · GOJO Industries, Inc.

Generic nameBenzalkonium Chloride
Dosage formLIQUID
RouteTOPICAL
Active ingredient(s)BENZALKONIUM CHLORIDE
Strength.5 mg/100mL
Marketing categoryOTC MONOGRAPH DRUG

Packages

21749-610-40 — 1200 mL in 1 PACKAGE (21749-610-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

21130-931 — Lidocaine HCL, Benzalkonium chloride, 21749-112 — Benzalkonium Chloride, 21749-113 — Benzalkonium Chloride, 21749-114 — Benzalkonium Chloride, 21749-359 — Benzalkonium Chloride Wipe, 21749-368 — BENZALKONIUM CHLORIDE, 21749-400 — Benzalkonium Chloride, 21749-454 — Benzalkonium Chloride, 21749-545 — Benzalkonium Chloride, 21749-607 — BENZALKONIUM CHLORIDE, 21749-684 — Benzalkonium Chloride, 21749-686 — Benzalkonium Chloride, 21749-687 — Benzalkonium Chloride, 21749-853 — Benzalkonium Chloride, 21749-968 — Benzalkonium Chloride, 23590-200 — Benzalkonium Chloride, 23590-300 — Benzalkonium Chloride, 23590-600 — Benzalkonium Chloride, 24286-1532 — BENZALKONIUM CHLORIDE, 26550-001 — BENZALKONIUM CHLORIDE, +1172 more

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