Zaliex Alcohol-Free Antiseptic Hand Sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

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Zaliex Alcohol-Free Antiseptic Hand Sanitizer

SAS Healthcare Inc

Zaliex Alcohol-Free Antiseptic Foam Hand Sanitizer


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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.

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

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

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

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

Zaliex Alcohol-Free Antiseptic Foam Hand Sanitizer 250ml (76452-003-00) | Zaliex Alcohol-Free Antiseptic Foam Hand Sanitizer 550ml (76452-003-01)

Zaliex Alcohol-Free Antiseptic Hand Sanitizer
Zaliex Alcohol-Free Antiseptic Hand Sanitizer

Zaliex Alcohol-Free Antiseptic Hand Sanitizer

BENZALKONIUM CHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76452-003
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.13 mg

Inactive Ingredients

Ingredient Name Strength
water
dihydroxypropyl PEG-5 linoleammonium chloride
GLYCERETH-2 COCOATE
BEHENTRIMONIUM CHLORIDE
dihydroxyethyl cocamine oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76452-003-00 250 in 1 BOTTLE
2 NDC:76452-003-01 550 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2012-09-13


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