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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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 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

  • 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 Red No. 33, FD&C Yellow No. 5.

Questions? Comments?

Call 1-800-228-4722

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

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

new

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

Touch of
Foam
ANTIBACTERIAL
HAND WASH

8.5 FL. OZ.
(251 mL)

rose &
cherry
in bloom

0388990

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label
LYSOL  TOUCH OF FOAM
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-465
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 RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-465-08251 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/26/201209/01/2020
2NDC:63824-465-11325 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/26/201209/01/2020
3NDC:63824-465-25739 mL in 1 BOTTLE; Type 0: Not a Combination Product12/26/201209/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/26/201209/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 5/2023
 
RB Health (US) LLC