Antiseptic Liquid
FDA Label NDC 79392-102
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Itimat Kozmetik Urunleri Sanayi Ve Ticaret Anonim Sirketi for the product Antiseptic Liquid (NDC 79392-102). 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, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
0,5% (w/w) Benzalkonium Chloride
Purpose
Antiseptic
Uses
• hand sanitizer to decrease bacteria on the skin
• recommended for repeated use
Warnings
For external use only
Do not use
• in children less than 2 months of age
• on open skin wounds
When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a doctor if
• irritation and redness develop
• condition persists for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• Squeeze a few pumps into your palms, foam with water and rinse.
• supervise children under 6 years of age when using this product to avoid swallowing
Other Information
• store between 15-30°C (59-86°F)
• avoid freezing and excessive heat above 40°C (104°F)
Inactive Ingredients
Deionised Water, Cocamidopropyl Betaine, Sodium Cocoamphoacetate, Lauryl Glucoside, Glycerin, PEG-150 Distearate, Hydrogenated Castor Oil,
Sodium Chloride, Citric Acid, CI 42090
Questions?
+1-646-301-0044
You may also report serious side effects to this phone number.
Mon-Fri 9:00 AM - 5:00 PM
Packaging
Image Description (79392102 2)
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