KLEENEX E2 FOAM SKIN CLEANSER- chloroxylenol solution

KLEENEX E2 Foam Skin Cleanser by

Drug Labeling and Warnings

KLEENEX E2 Foam Skin Cleanser 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

Chloroxylenol 1.75%

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on the skin.

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 or persists.

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

Directions

Wet hands and apply a palmful. Scrub thoroughly for 15-20 seconds. Rinse and dry thoroughly.

Other Information

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

Inactive Ingredients

Water, Hexylene Glycol, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Disodium EDTA, Sodium Hydroxide, MethylchloroisothiazoIinone, Methylisothiazolinone

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 - 1 Liter Container Label

Kleenex®
BRAND

E-2 Foam
Skin Cleanser

1 Liter (33.8 fl oz)

20-14-464-0-04

INGREDIENTS AND APPEARANCE

KLEENEX E2 FOAM SKIN CLEANSER 
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-570
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q)	Chloroxylenol	0.0175 L  in 1 L

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Hexylene Glycol (UNII: KEH0A3F75J)
Sodium Laureth Sulfate (UNII: BPV390UAP0)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Edetate Disodium (UNII: 7FLD91C86K)
Sodium Hydroxide (UNII: 55X04QC32I)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-570-10	1 L in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	05/15/2012

Labeler - Kimberly-Clark Corporation (006072136)