LYSOL NO TOUCH- benzalkonium chloride solution 
RB Health (US) LLC

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Lysol ®
No Touch™

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 ifirritation 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, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Methylchloroisothiazolinone/ Methylisothiazolinone, PPG-12-Buteth-16

Questions? Comments?

Call 1-800-228-4722

Reckitt Benckiser LLC
Parsippany, NJ 07054-0224
Made in U.S.A. © 2012 RB

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

Aloe Vera &
Vitamin E
With Moisturizers

Lysol ®
BRAND

KILLS 99.9% OF BACTERIA

No-Touch™
Refill

Antibacterial Hand Soap

0371649

8.5 FL. OZ. (251 mL)

Principal Display Panel - 251 mL Bottle Label
LYSOL  NO TOUCH
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-456
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-456-02251 mL in 1 BOTTLE; Type 0: Not a Combination Product11/30/201209/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00311/30/201209/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 10/2023
Document Id: 0710ef8e-6842-585b-e063-6294a90a5ac8
Set id: 3653edae-0919-43f4-8227-e25bf57069ff
Version: 2
Effective Time: 20231006
 
RB Health (US) LLC