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, Propylene Glycol, Citric Acid, Fragrance, Tetrasodium EDTA, Sodium Chloride, Hydrolyzed Collagen, PPG-12-Buteth-16, Magnesium Nitrate, Butylene Glycol, Phenoxyethanol, Methylchloroisothiazolinone, Magnesium Chloride, Ethylhexylglycerin, Methylisothiazolinone, FD&C Yellow No. 5, FD&C Yellow No. 6.

Questions? Comments?

Call 1-800-228-4722

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

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

NEW FORMULA!

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

Soft on Skin,
HARD ON GERMS ®

Antibacterial Hand Wash
No-Touch ®Refill

with
MOISTURIZING
COLLAGEN
COMPLEX

Odor Neutralizing Lemon & Verbena

8.5 FL. OZ. (251 mL)

8174292

Principal Display Panel - 251 mL Bottle Label
LYSOL  NO-TOUCH
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-489
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)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-489-02251 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/201509/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00406/01/201509/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 11/2023
Document Id: 0a4ab6fa-bf65-fe6e-e063-6394a90aa6fc
Set id: 1af7649c-7e61-4322-9a68-38cdae7a9691
Version: 2
Effective Time: 20231116
 
RB Health (US) LLC