Label: ENDURE 300 CIDA RINSE GEL ANTIMICROBIAL HAND RINSE- antiseptic handwash solution

  • NDC Code(s): 47593-264-26, 47593-264-31, 47593-264-33, 47593-264-49
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 12, 2024

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Ethyl Alcohol, 70%

  • Purpose

    Antiseptic hand wash

  • Uses

    • for hand washing to decrease bacteria on the skin
  • Warnings

    • For external use only
    • Flammable, keep away from fire or flame, heat, sparks and sources of static discharge.

    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 immediately.

  • Directions

    • apply product onto hands, spread thoroughly and rub until dry.
  • Other information

    • for additional information, see Material Safety Data Sheet (MSDS)
    • for emergency medical information in USA, call 1.800.328.0026
  • Inactive ingredients

    water (aqua), isopropyl alcohol, carbomer, propylene glycol, aminomethyl propanol, fragrance

  • QUESTIONS

    Questions? call 1.866.781.8787

  • Principal Display panel and representative label

    Ecolab®

    NDC 47593-264-26

    Endure® 300

    Cida-Rinse® Gel

    Antimicrobial Hand Rinse

    Active Ingredient:

    70% Ethyl Alcohol

    Net Contents:

    1000 mL (33.8 fl oz)

    61430349

    709409/8501/0311

    Ecolab • 370 Wabasha Street N • St Paul MN 55102-1390 USA

    © 2010 Ecolab USA Inc • All rights reserved

    Made in United States 709411/8501/1110 • SDS-OH-1518

    representative label

  • INGREDIENTS AND APPEARANCE
    ENDURE 300 CIDA RINSE GEL  ANTIMICROBIAL HAND RINSE
    antiseptic handwash solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-264
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-264-4937 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/22/199901/11/2011
    2NDC:47593-264-31540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/22/199907/14/2023
    3NDC:47593-264-261000 mL in 1 BAG; Type 0: Not a Combination Product11/22/1999
    4NDC:47593-264-33118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/22/199907/14/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/22/1999
    Labeler - Ecolab Inc. (006154611)