Alcohol Hand Sanitizer

Manufacturer
Tri-State Media, LLC | Genesis Chemical Canada
Effective date
2020-04-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:08:15

Label at a glance#

ProductAlcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure8 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 in your palm to thoroughly cover your hands and rub hands together until dry. Children under 6 years should be supervised when using this product.

Storage and handling

Store at a temperature below 43C (110F). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from source of heat, fire, or flame.

OTC - DO NOT USE SECTION

Do not use in children less than 2 months of age. Do not use on open skin wounds.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover your hands and rub hands together until dry.

Children under 6 years should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store at a temperature below 43C (110F).

May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Hydroxypropylcellulose (naturally derived), Glycerin, Isopropyl Myristate, Lauryl Lactate, Cetyl Lactate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

container labelcontainer labelAlcohol

Hand Sanitizer

with

Premium Skin Conditioners and Moisturizers

Contains

Ethyl Alcohol 80%

PRD# 99000736

Lot# 0040205

Expiry 04/2022

Net Contents: 4L

GenesisHealth

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN2
1039339ethanol 0.8 ML/ML Topical SolutionSCD2
1039339ethanol 80 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75784-001-012022-01-28C16284748780-1d6a99b39-8a8f-a426-e053-dadaa90af4c2a3fc0b3b-9250-35d2-e053-2a95a90afa96
75784-001-042022-01-28C16284748780-1d6a99b39-8a8f-a426-e053-dadaa90af4c2a3fc0b3b-9250-35d2-e053-2a95a90afa96

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75784-001-01Alcohol Hand Sanitizer1 L in 1 BOTTLESOLUTION12
75784-001-04Alcohol Hand Sanitizer4 L in 1 BOTTLESOLUTION42

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75784-001ALCOHOL HAND SANITIZER (ALCOHOL) SOLUTION [TRI-STATE MEDIA, LLC]2Legacy NDC, 2 package rows20200428_a3fc0b3b-9250-35d2-e053-2a95a90afa96.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
75784-00175784-001-04, 75784-001-01

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
a446bae0-e240-5aa0-e053-2995a90a3419a3fc0b3b-9250-35d2-e053-2a95a90afa962020-04-27WarningsExact identifier
spl id: a446bae0-e240-5aa0-e053-2995a90a3419
spl set id: a3fc0b3b-9250-35d2-e053-2a95a90afa96

Reported adverse events (FAERS/openFDA)#

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