Active ingredients

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Warnings

For external use only.

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

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

When using this product

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.

Keep out of reach of children

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

Stop use use and Seek

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

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

Uses

Hand sanitizer to help decrease bacteria on the skin.

When water, soap & towel are not available.

Recommended for repeated use.

Directions

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

Inactive Ingredients

Water

Glycerin

Carbomer

Propylene Glycol

Aminomethyl Propanol

Fragrance

Aloe（Aloe barbadensis）Leaf Juice

Tocopheryl Acetate

Hand Sanitizer 70% Ethyl Alcohol

Enriched with Moisturizing

Aloe Vera & Vitamin E

8 FL OZ(236ml)

Other information

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

Label

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label 2

label 3

AMERICAN RED CROSS 70% ETHYL ALCOHOL HAND SANITIZER
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75742-032
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:75742-032-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/21/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M003	03/21/2024

Labeler - Zhejiang Guoyao Jingyue Aerosol Co., Ltd (554529812)

Name	Address	ID/FEI	Business Operations
Establishment
Zhejiang Guoyao Jingyue Aerosol Co., Ltd.		554529812	manufacture(75742-032)