KLEENEX INSTANT HAND SANITIZER- alcohol solution

KLEENEX INSTANT HAND SANITIZER by

Drug Labeling and Warnings

KLEENEX INSTANT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Kimberly-Clark Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol 68% v/v

Purpose

Antiseptic

Use

Hand sanitizer to decrease bacteria on the skin.

Warnings

Flammable - Keep product away from fire or flame.

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 right away.

Directions

Wet hands thoroughly with product and allow to dry.

Other Information

• Report serious side effects from this product to 1-877-561-6587.
• Do not store above 110°F (40°C).

Inactive Ingredients

Water, Carbomer, Fragrance, Aminomethyl Propanol, Glycerin

Questions?

1-888-346-4652

SPL UNCLASSIFIED SECTION

Distributed in the U.S. by
Kimberly-Clark
Global Sales, LLC, Roswell,
GA 30076-2199

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

Kleenex®
BRAND
MARQUE

Instant Hand
Sanitizer

kills
germs†

8 fl oz (236 mL)

20-14-141-0-09

INGREDIENTS AND APPEARANCE

KLEENEX INSTANT HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-704
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	68 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-704-70	6 in 1 CARTON	08/30/2021
1	NDC: 55118-704-88	236 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M003	08/30/2021

Labeler - Kimberly-Clark Corporation (830997032)