LYSOL I.C. ANTIMICROBIAL- triclosan solution 
RB Health (US) LLC

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Lysol ®I.C.™
Antimicrobial Soap

Drug Facts

Active Ingredients

Triclosan 0.3%

Purpose

Health-care personnel handwash

Uses

For handwashing to decrease bacteria on the skin

Warnings

For external use only.

When using this product

  • Keep out of reach of children
  • Avoid contact with eyes. In case of eye contact, flush with water.
  • If irritation or redness develops, discontinue use immediately and consult a doctor.
  • If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

  • Wet hands with water.
  • Add soap and vigorously rub together all surfaces of lathered hands for at least 10 seconds.
  • Thoroughly rinse under a stream of water.
  • Dry thoroughly.

Other information

Store at room temperature. Keep from freezing.

Inactive ingredients

Citric Acid, Disodium Wheat Germamido PEG-2 Sulfosuccinate, Fragrance, Glycol Stearate, Lauramide DEA, Methylchloroisothiazolinone, Methylisothiazolinone, PEG-150 Distearate, Polyquaternium-7, Propylene Glycol, Sodium Chloride, Sodium Laureth Sulfate, Styrene/Acrylates Copolymer, Tallowaminopropylamine, Tetrasodium EDTA, Water

Questions? Comments?

Call 1-800-677-9218

Distributed by:
Reckitt Benckiser Inc., Parsippany, NJ 07054-0225

PRINCIPAL DISPLAY PANEL - 517.5 mL Bottle Label

READY-TO-USE

Lysol®
BRAND

I.C.™

Antimicrobial
Soap

Part of your
Infection Control
Program

  • Broad Spectrum
    Antimicrobial Effectiveness
  • Mild and Nondrying to Skin
  • Pleasant Fragrance

HEALTH CARE
PERSONNEL HANDWASH

ACTIVE INGREDIENT: 0.3% TRICLOSAN

NET CONTENTS: 17.5 FL. OZ. (517.5 mL)

Principal Display Panel - 517.5 mL Bottle Label
LYSOL I.C.  ANTIMICROBIAL
triclosan solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-499
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
GLYCOL STEARATE (UNII: 0324G66D0E)  
LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-499-51517.5 mL in 1 BOTTLE; Type 0: Not a Combination Product12/31/200409/01/2020
2NDC:63824-499-373790 mL in 1 BOTTLE; Type 0: Not a Combination Product12/31/200409/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00412/31/200409/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 11/2023
Document Id: 0a4b2aa3-214e-269e-e063-6394a90a1297
Set id: f3591efa-4bd6-4048-aef2-3fcec6b1d28d
Version: 2
Effective Time: 20231116
 
RB Health (US) LLC