Otc - Active Ingredient
Benzalkonium Chloride - 0.13%
Antibacterial
FDA Label NDC 78242-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Diamo Kozmetik Sanayi Ic Ve Dis Ticaret Limited Sirketi for the product Antibacterial (NDC 78242-004). 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, indications & usage, warnings for external use only, otc - stop use, when using this product, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose - Antibacterial
Indications & Usage
Use help eliminate bacteria on hands
Warnings For External Use Only
Causes serious eye damage. Toxic to aquatic life.Avoid release to the environment.
Dispose of contents/container in accordance with national regulations.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops
When Using This Product
Avoid contact with eyes.In case of contact, flush and rinse with water.
Remove contact lenses, if present and easy to do. Continue rinsing.
Keep Out Of Reach Of Children
Except under adult supervision. DO NOT EAT DRINK.
Keep away from food,drink and animal feeding stuffs,
If swallowed get medical help or contact posion control right away.
Directions
apply onto wet hands.
Lather and rinse thoeoughly.
Inactive Ingredient
Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Citric Acid, Glycerin, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4,Benzyl Alcohol,Cl 14720,Hexyl Cinnamal
* Please review the disclaimer below.
