Otc - Active Ingredient
Benzalkonium Chloride - 0.13%
Antibacterial
FDA Label NDC 50157-424
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 50157-424). 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, dosage & administration, warnings, otc - stop use, otc - when using, otc - keep out of reach of children, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Antibacterial
Dosage & Administration
Direction
- wet hands
- apply palmful to hands
- scrub thoroughly
- rinse
Warnings
Warning
For external use only - Hands only
Otc - Stop Use
Stop use and ask a doctor
- if irritation or redness develops
- condition persists for more than 72 hours.
Otc - When Using
When using this product
- avoid contact with eyes.
- If contact occurs, rinse eye thoroughly with water
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
Inactive Ingredient
Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Sodium Lauroamphoacetate , Polyquatemium-7, Citric Acid, Glycerin,
Aloe Barbadensis leaf Extract , Fragrance, Teocopheryl Acetate, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow# 5 (Cl 19140), Red# 40(Cl 16035)
Indications & Usage
Uses for handwashing or decrease bacteria to the skin
Package Label.Principal Display Panel
Lave (Lave)
Lave_2 (Lave 2)
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