LYSOL NO TOUCH- 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

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 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

• Wet hands
• Place hands under dispenser until soap is dispensed
• Wash hands
• Rinse hands with water
• Dry hands after rinsing

Other Information

store at room temperature

Inactive Ingredients

Water, Cetrimonium Chloride, Glycerin, PEG-150 Distearate, Lauramine Oxide, Cocamide MEA, Citric Acid, Fragrance,Tetrasodium EDTA, Sodium Chloride, Methylchloroisothiazolinone/ Methylisothiazolinone, PPG-12-Buteth-16, FD&C Red #4, D&C Orange #4

Questions? Comments?

Call 1-800-228-4722

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Reckitt Benckiser LLC
Parsippany, NJ 07054-0224

Made in U.S.A.

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

Refreshing
Grapefruit Essence™

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

No-Touch™
Refill

Antibacterial Hand Soap

8.5 FL. OZ. (251 mL)

0371646

INGREDIENTS AND APPEARANCE

LYSOL   NO TOUCH
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63824-455
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)
Cetrimonium Chloride (UNII: UC9PE95IBP)
Glycerin (UNII: PDC6A3C0OX)
PEG-150 Distearate (UNII: 6F36Q0I0AC)
Lauramine Oxide (UNII: 4F6FC4MI8W)
Coco Monoethanolamide (UNII: C80684146D)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Edetate Sodium (UNII: MP1J8420LU)
Sodium Chloride (UNII: 451W47IQ8X)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)
PPG-12-Buteth-16 (UNII: 58CG7042J1)
FD&C Red No. 4 (UNII: X3W0AM1JLX)
D&C Orange No. 4 (UNII: Q1LIY3BO0U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63824-455-02	251 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	11/30/2012

Labeler - Reckitt Benckiser LLC (094405024)