LYSOL  NO TOUCH- triclosan 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.

----------

Lysol®
No Touch™

Drug Facts

Active Ingredient

Triclosan 0.10%

Purpose

Antibacterial

Use

Helps kill bacteria on hands when used as a hand soap.

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

  • Place hands under dispenser until soap is dispensed.
  • Wash hands.
  • Rinse hands with water.

Other Information

store at room temperature

Inactive Ingredients

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Lauramine Oxide, Fragrance , Sodium Chloride, Sodium Cumenesulfonate, Citric Acid, Ethanolamine, Benzisothiazolinone, Methylisothiazolinone, FD&C Yellow No. 5, D&C Red No. 33

Questions? Comments?

1-800-228-4722

Distributed by: Reckitt Benckiser LLC
Parsippany, NJ 07054-0224

Hand Soap made in U.S.A.

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

sunkissed lemon
scent

Lysol®
BRAND
ANTIBACTERIAL HAND SOAP

No-Touch™
Kitchen System Refill
cleans dishes • surfaces • hands

160 dispenses

CONCENTRATED

0362166

8.5 FL.OZ. (251 mL)

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label
LYSOL   NO TOUCH
triclosan solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-470
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
Lauramine Oxide (UNII: 4F6FC4MI8W)  
Sodium Chloride (UNII: 451W47IQ8X)  
Sodium Cumenesulfonate (UNII: 5798KA13PG)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Monoethanolamine (UNII: 5KV86114PT)  
Benzisothiazolinone (UNII: HRA0F1A4R3)  
Methylisothiazolinone (UNII: 229D0E1QFA)  
FD&C Yellow No. 5 (UNII: I753WB2F1M)  
D&C Red No. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-470-01251 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E12/30/201204/01/2015
Labeler - Reckitt Benckiser LLC (094405024)

Revised: 6/2015
Document Id: a268aedf-376a-462f-9dbf-74cb409acb38
Set id: e0037f1d-4004-4aea-9e06-736248544a96
Version: 2
Effective Time: 20150602
 
Reckitt Benckiser LLC