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]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.10%

Purpose

Antibacterial

Use

for hand washing 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, Fragrance, Citric Acid, Acrylates/PEG-10 Maleate/Styrene Copolymer, Tetrasodium EDTA, Sodium Chloride, Methylchloroisothiazolinone/Methylisothiazolinone, PPG-12-Buteth-16, FD&C Yellow No. 5, D&C Orange No. 4, D&C Red No. 33, FD&C Blue No. 1.

Questions? Comments?

Call 1-800-228-4722

SPL UNCLASSIFIED SECTION

Made in U.S.A.

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

Vanilla Sugar
& Spice

LIMITED HOLIDAY COLLECTION

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

No -Touch™
Antibacterial
Hand Soap Refill

8.5 FL. OZ. (251 mL)

0344480

INGREDIENTS AND APPEARANCE

LYSOL   NO-TOUCH
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63824-476
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)
Methacrylate/Methoxy Peg-10 Maleate/Styrene Copolymer (UNII: 39DK5WQ2PR)
Edetate Sodium (UNII: MP1J8420LU)
Sodium Chloride (UNII: 451W47IQ8X)
PPG-12-Buteth-16 (UNII: 58CG7042J1)
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: 63824-476-01	1 in 1 BLISTER PACK
1		251 mL in 1 BOTTLE
2	NDC: 63824-476-02	200 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	01/23/2013

Labeler - Reckitt Benckiser LLC (094405024)