LYSOL NO TOUCH- benzethonium 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

Benzethonium chloride, 0.13%

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, Glycerin, Cetrimonium Chloride, Lauramide DEA, PEG-150 Distearate, Lauramine Oxide, Fragrance, Citric Acid, Tetrasodium EDTA, Benzophenone-4, Acrylates/PEG-10 Maleate/Styrene Copolymer, Di-PPG-2 Myreth-10 Adipate, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Yellow 5, D&C Orange 4, D&C Red 33 and FD&C Blue 1.

Questions? Comments?

Call 1-800-228-4722

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Reckitt Benckiser LLC
Parsippany, NJ 07054-0224

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

Creamy
Vanilla Bliss

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

No-Touch™
Refill

Antibacterial Hand Soap

8.5 FL. OZ. (251 mL)

0371628

INGREDIENTS AND APPEARANCE

LYSOL   NO TOUCH
benzethonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63824-462
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzethonium chloride (UNII: PH41D05744) (Benzethonium - UNII:1VU15B70BP)	Benzethonium chloride	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Cetrimonium Chloride (UNII: UC9PE95IBP)
Lauric Diethanolamide (UNII: I29I2VHG38)
PEG-150 Distearate (UNII: 6F36Q0I0AC)
Lauramine Oxide (UNII: 4F6FC4MI8W)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Edetate Sodium (UNII: MP1J8420LU)
Sulisobenzone (UNII: 1W6L629B4K)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)
FD&C Yellow No. 5 (UNII: I753WB2F1M)
D&C Orange No. 4 (UNII: Q1LIY3BO0U)
D&C Red No. 33 (UNII: 9DBA0SBB0L)
FD&C Blue No. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63824-462-02	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	09/15/2011

Labeler - Reckitt Benckiser LLC (094405024)