ETHYL ALCOHOL- alcohol gel

ETHYL ALCOHOL by

Drug Labeling and Warnings

ETHYL ALCOHOL by is a Otc medication manufactured, distributed, or labeled by ASP Global LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

DRUG FACTS

Each 100ml Contains

Active ingredient

Ethyl Alcohol I.P. :

PURPOSE

70.0% v/v Gel base

USES

Hand Sanitization to decrease bacteria on the skin.

For use when soap and water are not available.

WARNINGS

Flammable. Keep away from fire or flame.

For external use only. Recommended for repeated use.

WHEN USING THE 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, Keep out of reach of children. If swallowed, get medical help or call a poison control center.

DIRECTIONS

Not recommended for infants. Wet hands thoroughly with product & allow to self dry. Children under 6 years of age should be supervised when using this product.

OTHER INFORMATION

Avoid freezing, Do not store above 40°C ( 104°F ).

INGREDIENTS

Ultrez - 20. Glycerin, Propylene Glycol, Ethyl Alcohol, Aloe Vera Juice, Fragrance & Purified Water.

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY:

ASP GLOBAL, LLC
7800 THIRD FLAG PARKWAY,
AUSTELL, GA 30168, USA

PRINCIPAL DISPLAY PANEL - 53 mL Bottle Label

ASP
GLOBAL

INSTANT

Hand
Antiseptic

70.0% Ethyl Alcohol

1.9 FL OZ / 53 mL

INGREDIENTS AND APPEARANCE

ETHYL ALCOHOL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59448-011
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Glycerin (UNII: PDC6A3C0OX)
Propylene Glycol (UNII: 6DC9Q167V3)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S AT 0.5%) (UNII: YY2HMJ9NZF)
FRAGRANCE 13576 (UNII: 5EM498GW35)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59448-011-01	53 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M003	03/02/2025

Labeler - ASP Global LLC (080361159)