Alcohol free hand sanitizer

Manufacturer
Sanihealth Products Corporation
Effective date
2010-05-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:37

Label at a glance#

ProductAlcohol free hand sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Boxed warning

Warnings: For external use only. Keep out of reach of children. Avoid eye contact. Should contact occur, rinse thoroughly with water. If swallowed or irritation develops, discontinue use and consult a health care practitioner.

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION


Directions

Place a palmful (5 grams) in one hand. Spread onto both hands to wrist and rub into the skin until dry.

INACTIVE INGREDIENT SECTION


Water (Aqua), Decyl Glucoside, Glycerin, Fragrance, DMDM Hydantoin

BOXED WARNING SECTION


Warnings:

For external use only.

Keep out of reach of children.

Avoid eye contact. Should contact occur, rinse thoroughly with water.

If swallowed or irritation develops, discontinue use and consult a health care practitioner.

INDICATIONS & USAGE SECTION


Use

Use as part of your daily cleansing routine when soap and water are not available, or to supplement hand washing.

OTC - ACTIVE INGREDIENT SECTION


Active Ingredient                     Purpose

Benzalkonium Chloride 0.12%   Antiseptic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


labellabel

Mission Linen supply

Mission linen and uniform service

Alcohol free hand sanitizer

benzalkonium chloride 0.12%

High performance alcohol free foam hand sanitizer

1 L (33.8 U.S. OZ)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046310benzalkonium chloride 0.12 % Topical FoamPSN1
1046310benzalkonium chloride 1.2 MG/ML Topical FoamSCD1
1046310benzalkonium chloride 0.12 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51053-500-102019-10-21C16284748780-1956f9ecf-d18e-621f-e053-dbdaa90a74adAlcohol free hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51053-500-10Alcohol free hand sanitizer1000 mL in 1 BOTTLE, PUMPAEROSOL, FOAM10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51053-500ALCOHOL FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [SANIHEALTH PRODUCTS CORPORATION]1Legacy NDC, 1 package rows20100525_e079d60f-6811-410e-ad02-6e4072118bca.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W71
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51053-50051053-500-10

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
7b3f45f7-3757-49d2-8976-a33282db8c4fe079d60f-6811-410e-ad02-6e4072118bca2010-05-24Boxed warningExact identifier
spl id: 7b3f45f7-3757-49d2-8976-a33282db8c4f
spl set id: e079d60f-6811-410e-ad02-6e4072118bca

Reported adverse events (FAERS/openFDA)#

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