Sani-Foam Foaming Non-Alcohol Hand Sanitizer

Manufacturer: Multi-Clean
Effective date: 2025-01-17
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 20:42:06

Label at a glance#

ProductSani-Foam Foaming Non-Alcohol Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Indications and uses

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

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact651-481-1900

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, Dihydroxyethyl Cocamine Oxide, Acetamidoethoxyethanol, Citric Acid

Questions?

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label - 1 Gallon Pour Bottle

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62767-103	SANI-FOAM FOAMING NON-ALCOHOL HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [MULTI-CLEAN]	3	Unmatched	20250119_0d0991b5-b461-8465-e063-6394a90aeb2b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

Sani-Foam Foaming Non-Alcohol Hand Sanitizer
Benzalkonium Chloride
CITRIC ACID MONOHYDRATE
WATER
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE
DIHYDROXYETHYL COCAMINE OXIDE
BENZALKONIUM
ACETAMIDOETHOXYETHANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62767-103	62767-103-33, 62767-103-37

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE	H2KVQ74JM4	IACT
DIHYDROXYETHYL COCAMINE OXIDE	8AR51R3BL5	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
ACETAMIDOETHOXYETHANOL	LVX2APC4XR	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2bea1a96-aef8-3d60-e063-6394a90a110e			0d0991b5-b461-8465-e063-6394a90aeb2b	2025-01-17	Warnings	Exact identifier spl id: 2bea1a96-aef8-3d60-e063-6394a90a110e spl set id: 0d0991b5-b461-8465-e063-6394a90aeb2b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.