Otc - Active Ingredient
Benzalkonium Chloride
Soft Foam Hand Sanitizer
FDA Label NDC 80891-234
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Freedom Technologies Llc for the product Soft Foam Hand Sanitizer (NDC 80891-234). 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 - keep out of reach of children, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antibacterial
Indications & Usage
Antibacertial foaming hand cleaner. Use in daycare, nursing homes, restaurants, doctors offices, dental offices, schools and clinics
Warnings
For external use only. Avoid contact with eyes. If contact occurs, rinse with water. Discontinue use if irritation or redness develops. If irritation persist for more than 72 hours, consult a physician.
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.
Dosage & Administration
Ready to use without dilution. Dispense 1 pump of product onto plalm of hand and rub thoroughly over all surfaces of hands unitl dry.
Inactive Ingredient
Water, Decyl Glucoside, Glycerin, DMDM Hydantoin.
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