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

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

• For external use only
• Flammable
• Keep away from fire or flame

Do not use

• on children less than 2 months old
• on open skin wounds

When using this product

• keep out of eyes, ears, In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

• irritation or redness develops
• Condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

• Place enough product on hands to cover all surfaces.
• Rub hands together until dry
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Do not store above 105°F
• May discolor some fabrics
• Harmful to wood finishes and plastics

Inactive ingredients

aminomethyl propanol, carbomer homopolymer, glycerin, propylene glycol, purified water USP

Package Labeling:50count

Package Labeling:100count

INGREDIENTS AND APPEARANCE

ALCOHOL WET WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74979-005
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
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74979-005-01	50 in 1 CANISTER	08/20/2020
1		3.56 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 74979-005-02	100 in 1 CANISTER	08/20/2020
2		3.56 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)