Otc - Active Ingredient
Active Ingredient - Benzalkonium Chloride - 0.13%
Antibacterial
FDA Label NDC 50157-608
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Brands International Corporation for the product Antibacterial (NDC 50157-608). 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, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, 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 for handwashing to decrease bacteria on skin
Warnings
for external use only - hands only
Otc - When Using
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops.
Otc - Keep Out Of Reach Of Children
keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately
Dosage & Administration
Direction
* wet hands
* apply to hands
* scrub thoroughly
* rinse thoroughly
Inactive Ingredient
Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Vitamin E, Blue# 1, Yellow 5, Fragrance (Parfum)
Package Label.Principal Display Panel
8b (8b)
8 (8)
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