KLEENEX Luxury Foam Hand Sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

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KLEENEX Luxury Foam Hand Sanitizer

Kimberly-Clark Corporation

MARQUE Kleenex BRAND LUXURY FOAM HAND SANITIZER


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Use

Hand sanitizer to decrease bacteria on the skin. Recommended for repeated use.

Warnings

For External Use Only.

When using this product avoid contact with eyes; in case of contact, flush eyes with water.

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Other Information

  • Report serious side effects from this product to 1-877-561-6587

Directions

Pump enough foam product into your palm to cover your hands. Rub hands together briskly until dry. No rinsing required. Use as part of a daily cleaning routine.

Inactive / Non-medicinal Ingredients

Water, dihydroxypropyl PEG-5, linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide

Questions?

1-800-346-4652

Distributed in the U.S. by Kimberly-Clark Global Sales,
LLC, Roswell, GA 30076-2199
Distributed in Canada by Kimberly-Clark Inc.,
Mississauga, Ontario L5B 3Y5

PRINCIPAL DISPLAY PANEL - 1 Liter Container Label

Kimberly-Clark
PROFESSIONAL*

MARQUE
kleenex ®
BRAND

LUXURY FOAM HAND SANITIZER

Benzalkonium Chloride Solution, House Std., 0.1%

For Personal/Domestic Use Only

Fragrance Free • Alcohol Free

1 Liter
(33.8 fl oz)

NSF ®

Nonfood Compounds
Program Listed E3
143923

NDC: 055118-521-10
DIN: 02366045

20-14-559-0-01

KLEENEX Luxury Foam Hand Sanitizer

KLEENEX Luxury Foam Hand Sanitizer

Benzalkonium Chloride SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55118-521
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.001 g

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:55118-521-10 1000 in 1 CONTAINER
2 NDC:55118-521-12 1200 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2011-08-15


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