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Antimicrobial Foam Handwash

NDC 21749-416 · GOJO Industries, Inc.

Generic nameChlorhexidine Gluconate 2% Solution
Dosage formLIQUID
RouteTOPICAL
Active ingredient(s)CHLORHEXIDINE GLUCONATE
Strength20 mg/mL
Pharmacologic classDecreased Cell Wall Integrity [PE]
Marketing categoryNDA

Packages

21749-416-89 — 1200 mL in 1 BOTTLE (21749-416-89)

21749-416-90 — 1250 mL in 1 BOTTLE (21749-416-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

17271-107 — chlorhexidine gluconate, 17518-051 — Chlorhexidine Gluconate and Alcohol, 17518-082 — Chlorhexidine Gluconate and Isopropyl Alcohol, 17518-083 — Chlorhexidine Gluconate and Isopropyl Alcohol, 17856-0272 — Chlorhexidine Gluconate, 17856-2001 — Chlorhexidine Gluconate, 17856-2002 — Chlorhexidine Gluconate, 17856-2128 — Chlorhexidine Gluconate Oral Rinse, 21749-106 — Chlorhexidine Gluconate 2% Solution, 21749-225 — Chlorhexidine Gluconate 2% Solution, 21749-461 — Chlorhexidine Gluconate 2% Solution, 21749-850 — Chlorhexidine Gluconate 2%, 36800-401 — Chlorhexidine Gluconate 4%, 39892-0960 — Chlorhexidine Gluconate, 39892-0961 — Chlorhexidine Gluconate, 41250-162 — Chlorhexidine Gluconate 4%, 42939-124 — Chlorhexidine gluconate, 42939-125 — Chlorhexidine gluconate, 42939-127 — Chlorhexidine gluconate, 42939-128 — Chlorhexidine gluconate, +115 more

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