Active Ingredient
BENZALKONIUM CHLORIDE, 0.13%
Antibacterial Foam Solution
FDA Label NDC 11084-021
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sc Johnson Professional Usa Inc. for the product Antibacterial Foam (NDC 11084-021). 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, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
for handwashing to reduce bacteria on the skin
When Using This Product
avoid contact with eyes. In case of eye contact, flush with water.
Stop Use And Ask A Doctor If
irritation and redness develop and persist for more than 3 days.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
apply foaming cleanser to dry hands
rub hands together to spread lather
wash for 15-20 seconds
rinse & dry hands thoroughly
Inactive Ingredients
AQUA (WATER), GLYCERIN, LAURAMINE OXIDE, BUTYLENE GLYCOL, LACTIC ACID, SALICYLIC ACID, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI 19140).
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