ETHYL ALCOHOL WET WIPES- alcohol cloth

Ethyl alcohol wet wipes by

Drug Labeling and Warnings

Ethyl alcohol wet wipes by is a Otc medication manufactured, distributed, or labeled by ProStock LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol (70.00% V/V)

Purpose

Antiseptic

Uses

• For hand-washing to decrease bacteria on skin

Warnings

Flammable. Keep away from heat and flame.
For External use only.

Do not use

in eyes. In case of contact, rinse thoroughly with water.

Stop use & ask doctor

if rash/redness or irritation appears/develops and persist for more than 72 hours.

Keep out of reach from children

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

Directions

• Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation. 
• Thoroughly wipe hands, allow to dry without washing.
• Discard after single use

Other information

• Do not flush down toilet. 
• Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit) 
• May discolor certain fabrics

Inactive Ingredients

Aqua, Glycerin, Aloe Barbadensis Leaf Juice, D-Panthenol, Phenoxyethanol

Package Labeling:15pcs

Package Labeling:50pcs

INGREDIENTS AND APPEARANCE

ETHYL ALCOHOL WET WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73796-003
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)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DEXPANTHENOL (UNII: 1O6C93RI7Z)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73796-003-02	15 in 1 PACKAGE	08/20/2020
1		3.6 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 73796-003-03	50 in 1 PACKAGE	08/20/2020
2		3.6 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/20/2020

Labeler - ProStock LLC (078859574)