Active Ingredient
Benzalkonium Chloride 0.13%
Optisource Antibacterial Foam Hand
FDA Label NDC 64646-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Charlotte Products Ltd. for the product Optisource Antibacterial Foam Hand (NDC 64646-001). 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 active ingredient, purpose, uses, warnings, when using, stop using and ask doctor if, 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
Purpose
Antimicrobial
Uses
- For hand washing to decrease bacteria on the skin
- Recommended for repeated use
Warnings
For external use only
When Using
this product avoid contact with eyes. In case of eye contact, flush eyes with water.
Stop Using And Ask Doctor If
irritation or redness develops, or if 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
- Pump a small amount of foam into palm of hand
- Rub thoroughly over all surfaces of both hands for 15 seconds
- Rinse with potable water
Inactive Ingredient
Inactive Ingredients Water/Agua/Eau, Coco-glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric acid
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