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

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Lysol®
No Touch™

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 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, 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

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

Principal Display Panel - 251 mL Bottle Label
LYSOL  NO TOUCH
benzethonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-462
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-462-02251 mL in 1 BOTTLE; Type 0: Not a Combination Product09/15/201109/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00309/15/201109/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 10/2023
 
RB Health (US) LLC