ALCOHOL WET WIPES- alcohol cloth

Alcohol Wet Wipes by

Drug Labeling and Warnings

Alcohol Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Robert Gordon Ind. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 75% (v/v)

purpose

Antiseptic

Uses

• For hand sanitizing to decrease bacteria on the 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

When Using this product

• avoid contact with eyes and mouth. If in ayes, flush thoroughly with water.
• Discontinue use and contact a doctor if irritation and redness develop and conditions persis for more than 72 hours.

Keep out of reach of children

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

Directions

• Tear open packet and remove wipe.
• Wet hands thoroughly with product and let hands air dry.
• Throw used wipe in trash. Do not flush.

Inactive ingredient

Water

Other Information

• Store between 15-30 oC (59-86 oF)
• Avoid freezing and excessive heat above 40 oC (104 oF)

Package Labeling:10count

Package Labeling:40count

Package Labeling:80count

INGREDIENTS AND APPEARANCE

ALCOHOL WET WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74979-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74979-006-01	10 in 1 PACKAGE	08/20/2020
1		4.5 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 74979-006-02	40 in 1 PACKAGE	08/20/2020	04/15/2023
2		4.75 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 74979-006-03	80 in 1 PACKAGE	08/20/2020	04/15/2023
3		4.75 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 - Robert Gordon Ind. Ltd. (070064709)