LYSOL  TOUCH OF FOAM- benzalkonium chloride   
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®
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

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 Green No. 5, D&C Red No. 33.

Questions? Comments?

Call 1-800-228-4722

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

PRINCIPAL DISPLAY PANEL - Kit Package

Bonus Pack
Pump + Refill

8.5 FL. OZ. (251 mL)
25 FL. OZ. (1PT. 9 FL. OZ.) 739 mL
TOTAL: 33.5 FL. OZ. (2PT. 1.5 FL. OZ.) 990 mL

creamy
vanilla
orchid

Principal Display Panel - Kit Package
LYSOL   TOUCH OF FOAM
benzalkonium chloride kit
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63824-478
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63824-478-04 1 in 1 PACKAGE, COMBINATION
Quantity of Parts
Part # Package Quantity Total Product Quantity
Part 1 1 BOTTLE, PUMP 251 mL
Part 2 1 BOTTLE, PUMP 739 mL
Part 1 of 2
LYSOL   TOUCH OF FOAM
benzalkonium chloride solution
Product Information
Item Code (Source) NDC:63824-466
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.1 g  in 100 mL
Inactive Ingredients
Ingredient Name Strength
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 Green No. 5 (UNII: 8J6RDU8L9X)  
D&C Red No. 33 (UNII: 9DBA0SBB0L)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63824-466-08 251 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part333E 01/23/2013
Part 2 of 2
LYSOL   TOUCH OF FOAM
benzalkonium chloride solution
Product Information
Item Code (Source) NDC:63824-466
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.1 g  in 100 mL
Inactive Ingredients
Ingredient Name Strength
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 Green No. 5 (UNII: 8J6RDU8L9X)  
D&C Red No. 33 (UNII: 9DBA0SBB0L)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63824-466-25 739 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part333E 01/23/2013
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part333E 01/23/2013
Labeler - Reckitt Benckiser LLC (094405024)

Revised: 7/2013
Document Id: 81b449c5-d12a-4269-b632-33d64a0bc1bc
Set id: 08022415-b031-4b7d-8ff9-ab4803150405
Version: 1
Effective Time: 20130708
 
Reckitt Benckiser LLC