Label: KEYSTONE- triclosan solution

  • NDC Code(s): 47593-341-41, 47593-341-56
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 18, 2024

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  • Active ingredient

    Triclosan 0.3%

  • Purpose

    Antiseptic handwash

  • Uses

    • for handwashing to decrease bacteria on the skin
  • Warnings

    For external use only

    Do not use

    • in eyes

    When using this product

    • if in eyes, rinse promptly and thoroughly with water
    • discontinue use if irritation and redness develop

    Stop use and ask a doctor if

    • skin irritation or redness occurs for more than 72 hours

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • wet skins and apply a small amount on hands an forearms
    • scrub well, rinse thoroughly and dry
  • Other information

    • for additional information see, Safety Data Sheet (SDS)
    • for emergency medical information in USA and Canada, call 1.800.328.0026
  • INACTIVE INGREDIENT

    Inactive ingredients water (aqua), potassium cocoate, alcohol, sodium laureth sulfate, hexylene glycol, boric acid, cocamidopropyl PG-dimonium chloride phosphate, tetrasodium EDTA, cocamine oxide, fragrance, PEG-75 lanolin, methylparaben, propylparaben, aloe barbadensis leaf juice, FD&C blue 1

  • QUESTIONS

    Questions?  call 1.800.35.CLEAN (352.5326)

  • Principal display panel and representative label

    KEYSTONE

    ANTIBACTERIAL FOAM HANDSOAP

    Triclosan 0.3%

    SYSCO 0281531

    6100517 ECOLAB

    Net Contents:  1200 mL (40.6 US fl oz)

    750767/5401/0420

    Distributed by

    Sysco Corporation

    Manufactured by

    Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA ·

    tel: 1 800 35 CLEAN (352 5326)

    © 2020 Ecolab USA Inc · All rights reserved

    Made in U.S.A.

    representative label

  • INGREDIENTS AND APPEARANCE
    KEYSTONE 
    triclosan solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-341
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.3 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    BORIC ACID (UNII: R57ZHV85D4)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    COCAMINE OXIDE (UNII: QWA2IZI6FI)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-341-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/26/200005/03/2024
    2NDC:47593-341-561200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/26/2000
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/26/2000
    Labeler - Ecolab Inc. (006154611)
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