ETHYL ALCOHOL- alcohol liquid

ETHYL ALCOHOL by

Drug Labeling and Warnings

ETHYL ALCOHOL by is a Otc medication manufactured, distributed, or labeled by GOJO Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl alcohol 70%

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

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Flammable. Keep away from fire or flame.

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

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

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

Directions

Spray enough product in your palm to thoroughly cover and wet your hands
Rub hands together briskly until dry
Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Glyceryl Laurate, Tocopheryl Acetate, Fragrance (Parfum)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ETHYL ALCOHOL  
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21749-993
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL LAURATE (UNII: Y98611C087)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 21749-993-05	15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/20/2010
2	NDC: 21749-993-02	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/20/2010
3	NDC: 21749-993-08	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/20/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/20/2010	01/01/2022

Labeler - GOJO Industries, Inc. (004162038)

Registrant - GOJO Industries, Inc. (004162038)

Establishment
Name	Address	ID/FEI	Business Operations
GOJO Industries, Inc.		036424534	manufacture(21749-993)