Zaliex Alcohol-free Antiseptic Hand Sanitizer
FDA Label NDC 76452-003

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 Antiseptic Hand Sanitizer (NDC 76452-003). 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 antiseptic foam hand sanitizer, active ingredient, purpose, uses:, warnings:, otc - do not use, 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

Zaliex Alcohol-Free Antiseptic Foam Hand Sanitizer


Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses:

  • For hand cleansing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings:

For external use only.

Otc - Do Not Use

Do not use in eyes. If contact occurs, flush eyes with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develops.

If condition persists for more than 72 hours, consult a doctor.

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
  • Wet hands thoroughly with product and allow to dry without wiping.
  • 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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