LYSOL  NO-TOUCH- benzalkonium chloride solution 
Reckitt Benckiser 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

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 Blue #1

Questions? Comments?

Call 1-800-228-4722

Made in U.S.A.

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

Limited Edition

Sensitive
Skin

Dermatologically
Tested

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

No-Touch™
Refill

Antibacterial Hand Soap

Paraben Free • Triclosan Free

8.5 FL. OZ. (251 mL)

8105848

Principal Display Panel - 251 mL Bottle Label
LYSOL   NO-TOUCH
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-479
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 Blue No. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-479-02251 mL in 1 BOTTLE
2NDC:63824-479-011 in 1 BLISTER PACK
2251 mL in 1 BOTTLE, PLASTIC
3NDC:63824-479-033 in 1 BLISTER PACK
3251 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E12/01/2013
Labeler - Reckitt Benckiser LLC (094405024)

Revised: 12/2013
Document Id: c953a899-9e3c-48e8-9cf1-4eea4b9e6d1e
Set id: 0a794bef-ccaf-4c4f-85b7-a3b2ae2f6cf9
Version: 1
Effective Time: 20131203
 
Reckitt Benckiser LLC