LYSOL TOUCH OF FOAM- benzalkonium chloride 
RB Health (US) LLC

----------

Lysol ®
Touch of Foam

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.10%

Purpose

Antibacterial

Uses

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

  • Apply product to hands.
  • Wash hands.
  • Rinse hands with water.

Other Information

store at room temperature

Inactive Ingredients

Water, Glycerin, Lauramine Oxide, PEG-150 Distearate, Cetrimonium Chloride, Propylene Glycol, Fragrance, Citric Acid, Tetrasodium EDTA, Cocamide MEA, Methylchloroisothiazolinone, Methylisothiazolinone, D&C Green No. 5, D&C Red No. 33.

Questions? Comments?

Call 1-800-228-4722

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

PRINCIPAL DISPLAY PANEL - Kit Package

Bonus Pack
Pump + Refill

8.5 FL. OZ. (251 mL)
25 FL. OZ. (1PT. 9 FL. OZ.) 739 mL
TOTAL: 33.5 FL. OZ. (2PT. 1.5 FL. OZ.) 990 mL

creamy
vanilla
orchid

Principal Display Panel - Kit Package
LYSOL  TOUCH OF FOAM
benzalkonium chloride kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-478
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-478-041 in 1 PACKAGE, COMBINATION; Type 0: Not a Combination Product01/23/201309/01/2020
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE, PUMP 251 mL
Part 21 BOTTLE, PUMP 739 mL
Part 1 of 2
LYSOL  TOUCH OF FOAM
benzalkonium chloride solution
Product Information
Item Code (Source)NDC:63824-466
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)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-466-08251 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00301/23/2013
Part 2 of 2
LYSOL  TOUCH OF FOAM
benzalkonium chloride solution
Product Information
Item Code (Source)NDC:63824-466
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)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-466-25739 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00301/23/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00301/23/201309/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 10/2023
 
RB Health (US) LLC