Lysol No Touch (Benzalkonium Chloride) Solution [Reckitt Benckiser Llc] -

LYSOL NO TOUCH (BENZALKONIUM CHLORIDE) SOLUTION [RECKITT BENCKISER LLC]
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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, Propylene Glycol, Citric Acid, Fragrance, Tetrasodium EDTA, Sodium Chloride, Hydrolyzed Collagen, PPG-12-Buteth-16, Magnesium Nitrate, Butylene Glycol, Phenoxyethanol, Methylchloroisothiazolinone, Magnesium Chloride, Ethylhexylglycerin, Methylisothiazolinone, FD&C Yellow No. 5, FD&C Yellow No. 6.
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

Odor Neutralizing Lemon & Verbena

8.5 FL. OZ. (251 mL)

8174292

INGREDIENTS AND APPEARANCE

LYSOL NO TOUCH
benzalkonium chloride solution

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

Ingredient Name	Strength
Inactive Ingredients
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)
Sodium Chloride (UNII: 451W47IQ8X)
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)
Methylisothiazolinone (UNII: 229D0E1QFA)
FD&C Yellow No. 5 (UNII: I753WB2F1M)
FD&C Yellow No. 6 (UNII: H77VEI93A8)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:63824-489-02	251 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH NOT FINAL	part333E	06/01/2015

Labeler - Reckitt Benckiser LLC (094405024)

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