Otc - Active Ingredient
Active Ingredient Purpose
Benzethonium Chloride 0.2% ....................... Antibacterial
Unicowipes
FDA Label NDC 69652-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sabah Gida Saglik Temizlik Urunleri Dolum Ve Ambalaj Sana for the product Unicowipes (NDC 69652-000). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, 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
Otc - Purpose
Uses: decreases bacteria on skin
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Indications & Usage
Unicowipes
Warnings
Warnings:
For external use only
Do not use if you have allergic to any of the ingredients
When using this product do not get into eyes. If contact occurs, rinse thoroughly with water
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours
Dosage & Administration
Directions:
Tear the pack. Pull out the wet wipe.
Use wet wipe to clean hands, face or legs without soap or water and discard.
Inactive Ingredient
Inactive Ingredients
deionized water, cocoamido propyl betain, glycerin pharma, mono propylene glycol, PEG-7 glycery cocoate, polysorbate-20, fragrance, citric acid, benzyl alcohol, methylchloroisothiazolinone, methylisothiazolinone.
Package Label.Principal Display Panel
Label Image (Label)
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