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, Dan Mor. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium chloride

Keep our of the reach of children

Keep out of the reach of children, except with adult supervision.

Warnings

For external use only. Do not use in the eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult a doctor if irritation continues for more than 72 hours. If swallowed seek medical attention or call a poison control center.

Inactive ingredients

Aqua, Decyl Glucoside, Glycerin, Sodium Hydroxymethylglycinate, Citric Acid, PEG-12 Dimethicone Copolyol, Tetrasodium EDTA, Potassium Sorbate, Sodium Benzoate, Aloe Barbadensis Leaf Extract, Charmomilla Recutita (Matricaria),Flower Extract, Allantoin, Panthenol, Tocopheryl Acetate

Purpose

Antibacterial

To dispense

Locate tear-notch on top of refill pouch. Tear straight across to open. Pull first wipe from center of roll through the pouch center opening. Thread wipe through dispenser nozzle. Use only upward pull dispensers.

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74680-201-86	800 in 1 CANISTER	03/22/2024
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	03/22/2024

Labeler - Unico International Trading Corporation (805757200)

Registrant - Dan Mor (514523067)

Establishment
Name	Address	ID/FEI	Business Operations
Dan Mor		514523067	manufacture(74680-201)