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Endure 200 (Ecolab Inc.)

Available Formats

Dosage Form Package Information Links
SOLUTION 1000 mL in 1 BOTTLE, PLASTIC (47593-263-32) Label Information
SOLUTION 540 mL in 1 BOTTLE, PLASTIC (47593-263-31) Label Information

Complete Endure 200 Information

  • Active ingredient

    Triclosan, 1%


  • Purpose

    Healthcare personnel handwash


  • Uses

    • Healthcare personnel handwash

  • Warnings

    • For external use only

    Do not use
    • In eyes

    When using this product
    • If skin irritation and redness occurs, discontinue use.

    Stop use and ask doctor if
    • Skin irritation or redness persists 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 skin and spread a small amount on hands and forearms
    • Scrub well, rinse thoroughly and dry

  • Other Information

    • For emergency medical information in USA and Canada, call 1-800-328-0026.
    • For emergency medical information worldwide, call 1-651-222-5352 (in the USA).

  • INACTIVE INGREDIENT

    Inactive ingredients water, potassium cocoate, propylene glycol, glycerin, potassium stearate, tetrasodium EDTA, hydroxyethylcellulose, boric acid, cocamine oxide, fragrance, isopropyl alcohol, aloe barbadensis leaf juice, FDC green 3, FDC blue 1, FDC yellow 5


  • QUESTIONS

    Questions? Call 1-800-332-6522.


  • Principal Display Panel and Representative Label

    Hundtington brand

    NDC 47593-263-31

    DIN 02239250

    ENDURE​®â€‹ 200

    Healthcare Personnel Hand Wash

    Net Contents: 18 fl oz / 540 mL

    Skin Synergy​® ​Dermatology Management System

    represntative label


  • INGREDIENTS AND APPEARANCE
    ENDURE 200 
    triclosan solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-263
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 10.35 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM STEARATE (UNII: 17V812XK50)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)  
    BORIC ACID (UNII: R57ZHV85D4)  
    COCAMINE OXIDE (UNII: QWA2IZI6FI)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47593-263-32 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/20/1998 04/28/2018
    2 NDC:47593-263-31 540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/20/1998 04/28/2018
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 11/20/1998 04/28/2018
    Labeler - Ecolab Inc. (006154611)