Active Ingredient
Benzalkonium Chloride 0.1%
Sani-foam Foaming Non-alcohol Hand Sanitizer Solution
FDA Label NDC 62767-104
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Multi-clean for the product Sani-foam Foaming Non-alcohol Hand Sanitizer (NDC 62767-104). 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, otc - keep out of reach of children, directions, inactive ingredients, questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
- For handwashing to decrease bacteria on 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 use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Cener right away.
Directions
- Apply one pump of foam onto hands.
- Rub thoroughly over all surfaces of both hands.
- Rub hands together briskly until dry.
Inactive Ingredients
Water, Glycerin, Propylene Glycol, Phenoxyethanol, Lauramine Oxide, Panthenol, Citric Acid
Questions
651-481-1900 Monday - Friday 8:00 to 5:00 CT
Package Label.Principal Display Panel
Product Label (1 Gallon Short Neck Bottle)
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