USMed 70% Alcohol Gel Hand Sanitizer

Manufacturer
LTD ENTERPRISES DISTRIBUTION, INC.
Effective date
2020-06-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:14

Label at a glance#

ProductUSMed 70% Alcohol Gel Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

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 110°F (43°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

USMed 70% Alcohol Gel Hand Sanitizer

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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

Flammable. Keep away from source of heat, fire or flame.

For external use only.

Not for Consumption. Keep the product away from sunight.

When using this product

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 as these may be signs of a serious condition.

Keep out of reach of children

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 right away.

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.

Storage

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, carbomer, glycerine, triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 78072-500-

Made in Mexico

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78072-500-10USMed 70% Alcohol Gel Hand Sanitizer3790 mL in 1 JUGGEL37901
78072-500-11USMed 70% Alcohol Gel Hand Sanitizer118 mL in 1 BOTTLEGEL1181
78072-500-23USMed 70% Alcohol Gel Hand Sanitizer237 mL in 1 BOTTLEGEL2371
78072-500-47USMed 70% Alcohol Gel Hand Sanitizer473 mL in 1 BOTTLEGEL4731
78072-500-94USMed 70% Alcohol Gel Hand Sanitizer946 mL in 1 BOTTLEGEL9461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78072-500USMED 70% ALCOHOL GEL HAND SANITIZER (ALCOHOL) GEL [LTD ENTERPRISES DISTRIBUTION, INC.]1Legacy NDC, 5 package rows20200627_a8ff23cf-fb94-6756-e053-2a95a90aff19.zip

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
78072-50078072-500-10, 78072-500-11, 78072-500-23, 78072-500-47, 78072-500-94

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a8ff23cf-fb95-6756-e053-2a95a90aff19a8ff23cf-fb94-6756-e053-2a95a90aff192020-06-26WarningsExact identifier
spl id: a8ff23cf-fb95-6756-e053-2a95a90aff19
spl set id: a8ff23cf-fb94-6756-e053-2a95a90aff19

Reported adverse events (FAERS/openFDA)#

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