VALUE WIPES- benzalkonium chloride cloth

Value Wipes by

Drug Labeling and Warnings

Value Wipes by is a Otc medication manufactured, distributed, or labeled by Zogics, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antimicrobial

Uses

• For hand sanitizing to decrease the bacteria on the skin
• recommended for repated use

Warnings

For external use only

Do not use if allergic to any of these ingredients.

When using this product

avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor

If irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of the reach of children

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

Directions

• adults and childrens 2 years and older apply to hands; allow to dry without wiping
• children under 2 years ask a doctor

To dispense: Open Bad, remove the wipe

Other information

• store between 15°-30°C (59°F-86°F)
• avoid freezing and excessive heat above 40°C (104°F)
• keep closed tightly
• may discolor certain fabrics or surfaces

Inactive ingredients

Water, Phenoxyethanol, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis (Aloe) Leaf Extract, Decyl Glucoside, Disodium EDTA, Citric Acid, Fragrance.

Principal Display Panel

NDC: 72202-013-80

800 WIPES (8" X 6")

Zogic Value Wipes

Antibacterial Kills 99.99% of germs

Made in the USA from domestic & globally sourced materials

Reorder: ZV800 at zogics.com

DO NOT FLUSH

309 Pittsfield Road, Suite A, Lenox, MA 01240

INGREDIENTS AND APPEARANCE

VALUE WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72202-013
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 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72202-013-80	800 in 1 BAG	12/10/2024
1		1 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/10/2024

Labeler - Zogics, LLC (796321870)