Hand Sanitizer Gel

Manufacturer
The Source Design Collections
Effective date
2021-04-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:39:44

Label at a glance#

ProductHand Sanitizer Gel
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hands to cover all surfaces.Rub hands together until dry.

Storage and handling

Store in a cool dry place, away from direct sunlight and heat.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Antiseptic

Uses

DOSAGE & ADMINISTRATION SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

INACTIVE INGREDIENT SECTION

Water(aqua), propylene glycol, hydroxyethylcellulose, phenoxyethanol, alcohol

Directions

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces.Rub hands together until dry.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on open skin wounds or children under 2 months of age.

OTC - WHEN USING SECTION

When using this product keep out of eyes,ears, and mouth. ln case of contact with eyes,rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.These may be signs of a serious condition.

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 immediately.

Other information

STORAGE AND HANDLING SECTION

Store in a cool dry place, away from direct sunlight and heat.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1098199benzalkonium chloride 0.13 % Topical GelPSN2
1098199benzalkonium chloride 0.0013 MG/MG Topical GelSCD2
1098199benzalkonium chloride 0.13 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81726-002-012022-07-29C16284748780-1e4f33bdf-ae61-d8a0-e053-dadaa90a6e4ebfbdaa06-81af-abe2-e053-2a95a90ac3eb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81726-002-01Hand Sanitizer Gel100 mL in 1 TUBEGEL1002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81726-002HAND SANITIZER GEL GEL [THE SOURCE DESIGN COLLECTIONS]2Legacy NDC, 1 package rows20210417_bfbdaa06-81af-abe2-e053-2a95a90ac3eb.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81726-00281726-002-01

Ingredients#

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

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

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
c010d826-dfcf-387e-e053-2995a90a96babfbdaa06-81af-abe2-e053-2a95a90ac3eb2021-04-16WarningsExact identifier
spl id: c010d826-dfcf-387e-e053-2995a90a96ba
spl set id: bfbdaa06-81af-abe2-e053-2a95a90ac3eb

Reported adverse events (FAERS/openFDA)#

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