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 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, Fragrance, Propylene Glycol, Citric Acid, Tetrasodium EDTA, Acrylates/PEG-10 Maleate/Styrene Copolymer, Sodium Chloride, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Hydrolyzed Collagen, PPG-12-Buteth-16, Magnesium Nitrate, Butylene Glycol, Phenoxyethanol, Methylchloroisothiazolinone, Magnesium Chloride, Ethylhexylglycerin, Potassium Sorbate, Methylisothiazolinone, Sodium Benzoate.

Questions? Comments?

Call 1-800-228-4722

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

NEW FORMULA!

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

Soft on Skin,
HARD ON GERMS®
Antibacterial Hand Wash
No-Touch® Refill

with
MOISTURIZING
COLLAGEN
COMPLEX

Moisturizing Aloe & Vitamin E

8.5 FL. OZ. (251 mL)

8174294

INGREDIENTS AND APPEARANCE

LYSOL   NO TOUCH
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63824-488
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)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PPG-12-BUTETH-16 (UNII: 58CG7042J1)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63824-488-02	251 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	05/07/2015

Labeler - Reckitt Benckiser LLC (094405024)