Cleansol Antibacterial Wet Wipes
FDA Label NDC 78089-048
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Endeks Kimya Sanayi Ve Ticaret Anonim Sirketi for the product Cleansol Antibacterial Wet Wipes (NDC 78089-048). 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, uses, warnings, directions, other information, inactive ingredients, 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
Uses
To decrease bacteria on skin.
Warnings
For external use only
When using this product, avoid contacting eyes. In case of eye contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.
Directions
• Remove lid, open cap, thread wipe through slit and close lid.
• Gently remove wipe, clean skin thoroughly, and allow hands to dry.
• Do not flush, dispose in a waste basket, and close lid after use.
• Store at room temperature and protect from sun exposure.
• For children under 2 years old, ask a doctor before use.
Other Information
Production date, expiration date, and lot number are printed on the package.
Inactive Ingredients
Water, Phenoxyethanol, Peg 7 Glyceryl Cocoate, Polysorbate 20, Glycerin, Perfume (Lime Oil), Cocamidopropyl Betaine, Citric Acid, Limonene, Hexyl Cinnamal, Citral, Citronellol, Geraniol, Benzyl Benzoate, Linalool.
Packaging
Untitled (78089048 2)
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