DENATURED ALCOHOL- ethanol liquid

Denatured Alcohol by

Drug Labeling and Warnings

Denatured Alcohol by is a Otc medication manufactured, distributed, or labeled by Shantou Kangjie Daily Chemical Industry Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 75% v/v

PURPOSE

Antimicrobial

INDICATIONS & USAGE

Hand Sanitizer to help reduce bacteria on skin.

WARNING

Flammable liquid - Keep away from heat, spark, electrical, fire or flame.

Keep out of reach of children.

DO NOT USE

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

WHEN USING

When using this product,

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if irrtation or rash appears and lasts.

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

STOP USE

Stop use and ask doctor if irrtation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Place enough product in your palm to thoroughly spread on both hands.

Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENT

Purified Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DENATURED ALCOHOL 
ethanol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74047-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74047-003-32	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/06/2023
2	NDC: 74047-003-03	38 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/08/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/06/2023

Labeler - Shantou Kangjie Daily Chemical Industry Co.,Ltd (527128712)

Registrant - Shantou Kangjie Daily Chemical Industry Co.,Ltd (527128712)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou Kangjie Daily Chemical Industry Co.,Ltd		527128712	manufacture(74047-003)