LYSOL NO-TOUCH- 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 ®

No-Touch ® Antibacterial Hand Soap

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 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

  • 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, Citric Acid, Fragrance,Tetrasodium EDTA, Sodium Chloride, Methylchloroisothiazolinone/ Methylisothiazolinone, PPG-12-Buteth-16, FD&C Yellow No. 5, FD&C Yellow No. 6

Questions? Comments?

Call 1-800-228-4722

Made in U.S.A.

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

Odor
Neutralizing
Fresh Citrus
Squeeze

Lysol ®
BRAND
KILLS 99.9% OF BACTERIA

new

No-Touch®
Refill

Antibacterial Hand Soap

8.5 FL. OZ. (251 mL)

0377985

Principal Display Panel - 251 mL Bottle Label
LYSOL  NO-TOUCH
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-464
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)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-464-02251 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/201309/01/2020
2NDC:63824-464-011 in 1 BLISTER PACK07/01/201309/01/2020
2251 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/01/201309/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 5/2023
Document Id: fceeef6e-c93e-0384-e053-6294a90aa612
Set id: 58973739-316b-4ff5-8e4e-f6f0e423e203
Version: 2
Effective Time: 20230530
 
RB Health (US) LLC