Zaliex Alcohol-free Foaming Hand Sanitizer
FDA Label NDC 76452-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sas Healthcare Inc for the product Zaliex Alcohol-free Foaming Hand Sanitizer (NDC 76452-004). 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 zaliex alcohol-free foaming hand sanitizer, active ingredient, purpose, uses:, warnings:, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.1%
Purpose
Antimicrobial
Uses:
For hand sanitizing, to eliminate harmful bacteria and germs on skin.Use as part of your daily cleansing routine.Recommended for repeated use.
Warnings:
For external use only.
Otc - When Using
When using this product avoid contact with eyes. In case of eye contact, flush with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops, or if condition persists.
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.
Directions:
- Pump a small amount of foam into palm of hand
- Run thoroughly over all surfaces of both hands
- Rub hands together briskly until dry
Inactive Ingredients:
Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance
Manufactured For:
Zaliex
Suite 210, 4 Robert Speck Parkway,
Mississauga, Ontario, L4Z1S1, Canada
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