Active Ingredient
Benzalkonium chloride
Wipex Cloth
FDA Label NDC 74680-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Unico International Trading Corporation for the product Wipex (NDC 74680-201). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, keep our of the reach of children, warnings, inactive ingredients, purpose, to dispense, to use, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
* Please review the disclaimer below.
