LYSOL TOUCH OF FOAM- benzalkonium chloride solution

Lysol by

Drug Labeling and Warnings

Lysol by is a Otc medication manufactured, distributed, or labeled by Reckitt Benckiser LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active Ingredient

Benzalkonium Chloride 0.10%

Purpose

Antibacterial

Uses

for handwashing to decrease bacteria on the skin

Warnings

For external use only

When using this product

• Avoid contact with eyes.
• In case of eye contact, flush with water.

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

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

Directions

• Apply product to hands.
• Wash hands.
• Rinse hands with water.

Other Information

store at room temperature

Inactive Ingredients

Water, Glycerin, Lauramine Oxide, PEG-150 Distearate, Cetrimonium Chloride, Propylene Glycol, Fragrance, Citric Acid, Tetrasodium EDTA, Cocamide MEA, Methylchloroisothiazolinone, Methylisothiazolinone, D&C Green No. 5, D&C Red No. 33.

Questions? Comments?

Call 1-800-228-4722

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Distributed by: Reckitt Benckiser LLC
Parsippany, NJ 07054-0224
Made in U.S.A.

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

new

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

Touch of
Foam™
ANTIBACTERIAL
HAND WASH

8.5 FL. OZ.
(251 mL)

creamy
vanilla
orchid

0389679

INGREDIENTS AND APPEARANCE

LYSOL   TOUCH OF FOAM
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63824-466
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Lauramine Oxide (UNII: 4F6FC4MI8W)
PEG-150 Distearate (UNII: 6F36Q0I0AC)
Cetrimonium Chloride (UNII: UC9PE95IBP)
Propylene Glycol (UNII: 6DC9Q167V3)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Edetate Sodium (UNII: MP1J8420LU)
Coco Monoethanolamide (UNII: C80684146D)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)
D&C Green No. 5 (UNII: 8J6RDU8L9X)
D&C Red No. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63824-466-08	251 mL in 1 BOTTLE, PUMP
2	NDC: 63824-466-11	325 mL in 1 BOTTLE, PUMP
3	NDC: 63824-466-25	739 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	12/26/2012

Labeler - Reckitt Benckiser LLC (094405024)