FDA.reportPublic FDA data

SANIMOR ALCOHOL-FREE FOAMING HAND SANITIZER

Manufacturer
Avmor
Effective date
2018-11-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:47:46

Label at a glance#

ProductSANIMOR ALCOHOL-FREE FOAMING HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For personal hand hygiene to help decrease bacteria on skin.

Dosage and administration

Pump a small amount of Foaming Hand Sanitizer into the palm of your hand. Rub product onto hands and allow to dry.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride, 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

For personal hand hygiene to help decrease bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. Should this occur, flush eyes with water.

Stop use and consult a physician

OTC - STOP USE SECTION

If irritation or redness develop, or if condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

 Directions

DOSAGE & ADMINISTRATION SECTION

Pump a small amount of Foaming Hand Sanitizer into the palm of your hand.

Rub product onto hands and allow to dry.

 Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Lauryldimethylamine Oxide.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sanimor

Alcohol Free

Foaming

Hand Sanitizer

1L 33.8 FL OZ

Container LabelContainer Label

Sanimor

Alcohol Free

Foaming

Hand Sanitizer

250mL 8.4 FL OZ

250mL container label250mL container label

SPL UNCLASSIFIED SECTION

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63937-236463937-2364-1, 63937-2364-2, 63937-2364-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LAURAMINE OXIDE4F6FC4MI8WIACT

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
cc0cb827-6cc9-82d2-e053-2995a90ab45592d1db55-66e2-468b-ac18-8e4e0d3739d72021-09-15WarningsExact identifier
spl set id: 92d1db55-66e2-468b-ac18-8e4e0d3739d7

Reported adverse events (FAERS/openFDA)#

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