Sani-Foam Foaming Non-Alcohol Hand Sanitizer

Manufacturer
Multi-Clean
Effective date
2025-10-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:39:54

Label at a glance#

ProductSani-Foam Foaming Non-Alcohol Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 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.

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 Cener 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, Glycerin, Propylene Glycol, Phenoxyethanol, Lauramine Oxide, Panthenol, 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 Short Neck BottleProduct Label - 1 Gallon Short Neck Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN2
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD2
1038799benzalkonium chloride 0.1 % Topical FoamSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62767-104-31Sani-Foam Foaming Non-Alcohol Hand Sanitizer50 mL in 1 BOTTLE, PUMPSOLUTION502
62767-104-33Sani-Foam Foaming Non-Alcohol Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICSOLUTION37852
62767-104-37Sani-Foam Foaming Non-Alcohol Hand Sanitizer208198 mL in 1 DRUMSOLUTION2081982
62767-104-39Sani-Foam Foaming Non-Alcohol Hand Sanitizer50 mL in 1 BOTTLE, PUMPSOLUTION502
62767-104-39Sani-Foam Foaming Non-Alcohol Hand Sanitizer24 in 1 BOXSOLUTION242

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62767-10462767-104-33, 62767-104-37, 62767-104-31, 62767-104-39

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-01-17full-release2026-06-01 00:53:01

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sani-Foam Foaming Non-Alcohol Hand SanitizerBENZALKONIUM CHLORIDEMulti-Clean2bea7ec7-e79e-8f34-e063-6294a90a96092025-10-23WarningsExact identifier
ndc (package): 62767-104-33
ndc (package): 62767-104-39
ndc (package): 62767-104-37
ndc (package): 62767-104-31
ndc (product): 62767-104
ndc11 (package): 62767010433
ndc11 (package): 62767010431
ndc11 (package): 62767010439
ndc11 (package): 62767010437
spl id: 41d9312a-863e-6139-e063-6294a90ae1bf
spl set id: 2bea7ec7-e79e-8f34-e063-6294a90a9609

Reported adverse events (FAERS/openFDA)#

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