WIPEX- antibacterial wipe cloth

Wipex by

Drug Labeling and Warnings

Wipex by is a Otc medication manufactured, distributed, or labeled by Unico International Trading Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium chloride 0.13%

Keeo Out of the Reach of Children

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Contrl right away.

Warning

For external use only. Avoid cntact with the eyes. If in eyes, flush thoroughly with water.

Inactive Ingredients

Sodium benzoate, sodium chloride, citric acid, potassium sorbate, sodium hydroxymethylglycinate, aloe vera, water

Purpose

Antiseptic

To disperse

To begin: Break tab on bucket rim and pull off cover. Open bag inside to expose wipes, then thread center wipe through the lid. Replace bucket cover to maintain moisture.

Stop Use

Stop and ask a doctor if:

Irritation or redness developes.

Conditions persists for more than 72 hours.

To Use

Sanitize hands or other affected area. Discard in trash after use.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WIPEX 
antibacterial wipe cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74680-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74680-201-63	400 in 1 CANISTER	11/04/2024
1	NDC: 74680-201-91	2.4 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 Drug	M003	11/04/2024

Labeler - Unico International Trading Corporation (805757200)