Breeze Antibacterial Wet Wipes 60 Pcs
FDA Label NDC 74955-021
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cosmolive Kozmetik Sanayi Ve Ticaret Anonim Sirketi for the product Breeze Antibacterial Wet Wipes 60 Pcs (NDC 74955-021). 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 drug facts, active ingredient, purpose, warnings, directions for use, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.13%
Purpose
Antibacterial
Warnings
For external use only
Keep out of eyes. In case of eye contact, rinse with water.
If irritation develops, discontinue use.
Consult a doctor if irritation persists more than 72 hours.
If swallowed, seek medical attention or contact a Poison Control Center.
Directions For Use
Thoroughly wipe hands and face as desired.
Allow to dry without wiping.
Discard wipe in trash receptacle after use. Do not flush.
Inactive Ingredients
Aqua, Phenoxyethanol, Perfume, Propylene Glycol, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Benzoic acid, Tetrasodium Edta, Dehydroacetic acid, Glycerin, Tocopheryl Acetate (Vit E), Aloe Barbadensis Leaf Extract (Aloevera), Polysorbate 20, Citric Acid.
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