SANI-FOAM FOAMING NON-ALCOHOL HAND SANITIZER- benzalkonium chloride solution

Sani-Foam Foaming Non-Alcohol Hand Sanitizer by

Drug Labeling and Warnings

Sani-Foam Foaming Non-Alcohol Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Multi-Clean. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

• For handwashing to decrease bacteria on skin.
• Recommended for repeated use.

Warnings

For external use only.

When using this product, avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Cener right away.

Directions

• Apply one pump of foam onto hands.
• Rub thoroughly over all surfaces of both hands.
• Rub hands together briskly until dry.

Inactive Ingredients

Water, Glycerin, Propylene Glycol, Phenoxyethanol, Lauramine Oxide, Panthenol, Citric Acid

Questions

651-481-1900 Monday - Friday 8:00 to 5:00 CT

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SANI-FOAM FOAMING NON-ALCOHOL HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62767-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
PANTHENOL (UNII: WV9CM0O67Z)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Product Characteristics
Color	white (water white - colorless, dispensed as white foam)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62767-104-33	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/17/2025
2	NDC: 62767-104-37	208198 mL in 1 DRUM; Type 0: Not a Combination Product	01/17/2025
3	NDC: 62767-104-31	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/23/2025
4	NDC: 62767-104-39	24 in 1 BOX	10/23/2025
4		50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/17/2025

Labeler - Multi-Clean (005115852)