LYSOL  TOUCH OF FOAM- 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®
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 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 Type HUMAN OTC DRUG Item Code (Source) NDC:63824-465
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 Red No. 33 (UNII: 9DBA0SBB0L)  
FD&C Yellow No. 5 (UNII: I753WB2F1M)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63824-465-08 251 mL in 1 BOTTLE, PUMP
2 NDC:63824-465-11 325 mL in 1 BOTTLE, PUMP
3 NDC:63824-465-25 739 mL in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part333E 12/26/2012
Labeler - Reckitt Benckiser LLC (094405024)

Revised: 11/2012
Document Id: cc9c6315-7e29-4266-baf9-74bbde06da75
Set id: af387105-c200-4665-a702-9210d39cb4db
Version: 1
Effective Time: 20121121
 
Reckitt Benckiser LLC