WIPESPLUS HAND SANITIZING WIPES- ethyl alcohol cloth

Wipesplus Hand Sanitizing Wipes by

Drug Labeling and Warnings

Wipesplus Hand Sanitizing Wipes 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

• For hand sanitizing to decrease bacteria on the skin.
• Apply topically to the skin to help prevent cross contamination
• Not recommended for repeated use.
• Dries in seconds.

Warnings

For external use only.

Flammable, keep away from fire or flame.

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 and redness develop
• 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

• Remove lid.
• Pull wipe from center of roll and thread theough opening in lid. Do not push finger through opening.
• Replace lid, pull wipe up, and then at 45° angle. The next wipe dispenses automatically.
• Close lid to retain moisture.

Other Information

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

Inactive Ingredients

Aloe Barbadensis Extract, Benzalkonium Chloride, Citric Acid, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Water

Principal Display Panel

wipesplus

HAND SANITIZING WIPES

• Killes 99.9% of germs

240 CT

INGREDIENTS AND APPEARANCE

WIPESPLUS HAND SANITIZING WIPES 
ethyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67151-737
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67151-737-01	240 in 1 PACKAGE; Type 0: Not a Combination Product	07/13/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/13/2022

Labeler - Progressive Products, LLC (127111792)