American Red Cross 70% Ethyl Alcohol Hand Sanitizer

Manufacturer
Zhejiang Guoyao Jingyue Aerosol Co., Ltd | Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Effective date
2026-01-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:31:35

Label at a glance#

ProductAmerican Red Cross 70% Ethyl Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help decrease bacteria on the skin. When water, soap & towel are not available. Recommended for repeated use.

Dosage and administration

Pump as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat sparks, electrical, fire or flame.

OTC - DO NOT USE SECTION

Do not apply around eyes.Do not use in ears & mouth.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. In case of eye contact remove any contact lenses, and flush eyes with cold water. call a poison center or doctor/ physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children must be supervised in use of this product.

OTC - STOP USE SECTION

Stop use use and Seek Medical sdvisement if irritation and Redness develop.

OTC - ASK DOCTOR SECTION

If swallowed, do not induce vomiting. Seek immediate medical attention.

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin.

When water, soap & towel are not available.

Recommended for repeated use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump as needed into your palms and thoroughly spread on both hands.
  • Rub into skin until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

Glycerin

Carbomer

Triethanolamine

Aloe barbadensis leaf extract

Hand Sanitizer 70% Ethyl Alcohol

SPL UNCLASSIFIED SECTION

Enriched with Moisturizing

Aloe Vera & Vitamin E

8 FL OZ(236ml)

Other information

SPL UNCLASSIFIED SECTION

  • Store at 20ºC(68-77ºF)
  • May discolor fabrics
  • Questions/ Comment? Call toll-free:1-877-879-6999

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75742-018-012026-01-05C16284748780-12cef2736-b184-d83d-e063-dadaa90ab31ff6bf5c5a-4954-4030-e053-6394a90a9cba
75742-018-012025-01-30C16284748780-12cef2736-b184-d83d-e063-dadaa90ab31ff6bf5c5a-4954-4030-e053-6394a90a9cba

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75742-018-01American Red Cross 70% Ethyl Alcohol Hand Sanitizer236 mL in 1 BOTTLE, PUMPGEL2362

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
75742-01875742-018-01

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
American Red Cross 70% Ethyl Alcohol Hand SanitizerETHYL ALCOHOLZhejiang Guoyao Jingyue Aerosol Co., Ltdf6bf5c5a-4954-4030-e053-6394a90a9cba2026-01-05WarningsExact identifier
ndc (package): 75742-018-01
ndc (product): 75742-018
ndc11 (package): 75742001801
spl id: 47afc5cc-4c6a-e2be-e063-6394a90a03ca
spl set id: f6bf5c5a-4954-4030-e053-6394a90a9cba

Reported adverse events (FAERS/openFDA)#

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