FDA.reportPublic FDA data

Sani-Foam Foaming Non-Alcohol Hand Sanitizer

Manufacturer
Multi Clean
Effective date
2023-12-21
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:17:25

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 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, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, 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

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62767-10262767-102-33, 62767-102-37

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
GLYCERETH-17 COCOATE3057VPT0KCIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0d0aca6a-61e3-c65e-e063-6294a90a6cf8fd022d96-8f06-4c7b-910b-52a42ecf6c542023-12-21WarningsExact identifier
spl id: 0d0aca6a-61e3-c65e-e063-6294a90a6cf8
spl set id: fd022d96-8f06-4c7b-910b-52a42ecf6c54

Reported adverse events (FAERS/openFDA)#

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