ETHYL ALCOHOL- hand sanitizing wipes cloth

Ethyl Alcohol by

Drug Labeling and Warnings

Ethyl Alcohol by is a Otc medication manufactured, distributed, or labeled by Progressive Products, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

• Hand sanitizing wipes to help reduce bacteria on the skin.

Warnings

For External use only.

Flammable

Keep away from fire or flame.

Do not use

• in or near the eyes
• on open skin wounds or burns

Stop use and ask a doctor

• if irritation or redness develops
• condition persists or get worse

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• Pull back canster lid
• Remove wipe
• Close canister lid
• Keep lid closed to retain moisture
• Wet hands thoroughly with product and allow to dry without wiping
• For single use only. Discard individual wipe after use

Other information

• Store at room temperature
• Dispose of used wipe in trash, do not flush into toilet.

Inactive ingredients

Water, Propylene Glycol, Glycerin, Fragrance, Benzalkonium chloride, Tocopherol Acetate, Citric Acid, Aloe Barbadensis Leaf Juice

Principal Display Panel

WAXIE

Hand Sanitizing Wipes

70% Alcohol Based

Kills 99.9% of germs

12/240 CT CANISTERS

INGREDIENTS AND APPEARANCE

ETHYL ALCOHOL 
hand sanitizing wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67151-738
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67151-738-01	240 in 1 BOX	03/13/2023
1		1 mL in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/13/2023

Labeler - Progressive Products, LLC (127111792)