WIPESPLUS SANITIZING ALCOHOL FREE WIPES- benzalkonium chloride cloth

Wipesplus Sanitizing Alcohol Free Wipes by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

• For hand sanitizing to decrease bacteria on the skin.
• Apply topically to the skin to help prevent cross contamination.
• Recommended for repeated use.
• Dries in seconds.

Warnings

• For external use only.
• May irritate eyes.

Keep out of the reach of children unless under adult supervision

Keep out of the reach of children unless under adult supervision

Directions

• Tear V notch on top of plastic bag.
• Pull first wipe from the center of roll up through opening of bag.
• Thread first wipe through the dispensing nozzle in lid of floor stand or
• Thread first wipe through dispensing nozzle in top of wll mounted dispenser.
• Close dispenser door. Wipe dispensing tension may be adjusted on top of dispenser. Dispenser must be mounted with wipes dispensing up.

Inactive Ingredient

Purified Water, Polysorbate 20, Glycerin, Phenoxyethanol, Sodium Benzoate, Citric Acid, Fragrance, Potassium Sorbate, Decyl Glucoside, Ethylhexylglycerin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice.

Principal Display Panel

Wipesplus

SANITIZING ALCOHOL FREE WIPES

Kills 99.9% of germs

240CT

1500CT

800CT

400CT

INGREDIENTS AND APPEARANCE

WIPESPLUS SANITIZING ALCOHOL FREE WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67151-343
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67151-343-01	240 in 1 CANISTER; Type 0: Not a Combination Product	07/13/2022
2	NDC: 67151-343-02	1500 in 1 PACKAGE; Type 0: Not a Combination Product	07/13/2022
3	NDC: 67151-343-03	800 in 1 PACKAGE; Type 0: Not a Combination Product	07/13/2022
4	NDC: 67151-343-04	400 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	part333A	07/13/2022

Labeler - Progressive Products, LLC (127111792)