anti-bacterial hand gel

Manufacturer
UniGroup Wholesale Inc.
Effective date
2016-03-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:45:32

Label at a glance#

Productanti-bacterial hand gel
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Other Information: Store below 118 F.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:
Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Purpose Antiseptic

WARNINGS SECTION

Warnings:For external use only.

Flammable. Keep away from fire or flame.

OTC - STOP USE SECTION

Stop use and ask for a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a doctor right away.

DOSAGE & ADMINISTRATION SECTION

Directions:
Pump as needed into your palms to cover hands. Rub hands together briskly until dry. Children under 6 years old should be supervised when using this product.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Aloe Barbadensis Leaf Juice, Glycerin, Propylene Glycol, Fragrance, Carbomer, Aminomethyl Propanol, Lactose, Microcrystalline Cellulose, Sucrose, Zea Mays (corn) Starch, Ultramarine Blue CI 77007, Tocopheryl Acetate, Hydroxpropyl Methyl Cellulose, FD&C Blue No.1, FD&C Yellow No.5, FD&C Red No.33, FD&C Red No.4.

STORAGE AND HANDLING SECTION

Other Information: Store below 118 F.

INDICATIONS & USAGE SECTION

UseTo help reduce bacteria on the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69358-0020-12023-01-30C16284748780-1f386c649-caa9-0266-e053-dadaa90a7c1a2ed6cf01-01b4-04af-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69358-0020-1anti-bacterial hand gel29 mL in 1 BOTTLE, SPRAYGEL291

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69358-0020ANTI-BACTERIAL HAND GEL (ETHYL ALCOHOL) GEL [UNIGROUP WHOLESALE INC.]1Legacy NDC, 1 package rows20160325_2ed6cf01-01b4-04af-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69358-002069358-0020-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
2ed6cf01-01b5-04af-e054-00144ff88e882ed6cf01-01b4-04af-e054-00144ff88e882016-03-24WarningsExact identifier
spl id: 2ed6cf01-01b5-04af-e054-00144ff88e88
spl set id: 2ed6cf01-01b4-04af-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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