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

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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, Hydrolyzed Collagen, Magnesium Nitrate, Butylene Glycol, Phenoxyethanol, Methylchloroisothiazolinone, Magnesium Chloride, Ethylhexylglycerin, Methylisothiazolinone, D&C Red 33, FD&C Yellow 5.

Questions? Comments?

Call 1-800-228-4722

Distributed by:
Reckitt Benckiser
Parsippany, NJ 07054-0224

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

NEW FORMULA!

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

Soft on Skin,
HARD ON GERMS ®

Antibacterial
Foam Hand Wash

with
MOISTURIZING
COLLAGEN
COMPLEX

8.5 FL. OZ.
(251 mL)

Rose & Cherry in Bloom

8170158

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label
LYSOL  TOUCH OF FOAM
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-486
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)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-486-01251 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/21/201509/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00404/21/201509/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 11/2023
Document Id: 0a4a8db8-da0f-efa3-e063-6394a90a347a
Set id: 0d61fa1b-98ac-463a-a145-17013b7df5d6
Version: 2
Effective Time: 20231116
 
RB Health (US) LLC