Label: FENDALL 2000 PURE FLOW- purified water liquid

  • NDC Code(s): 0498-0631-37
  • Packager: Honeywell Safety Products USA, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 6, 2024

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  • Active ingredient

    Purified Water 98.6%

  • Purpose

    Emergency Eyewash

  • Uses

    For flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination

  • Warnings

    For external use only

    • store at room temperature, 59 o to 86 oF (15 o to 30 oC)
    • do not freeze

    Do not use

    • if solution changes color or gets cloudy
    • in open wounds in or near the eyes
    • with contact lenses

    Stop use and ask a doctor if you have

    • changes in vision
    • eye pain
    • continued redness, irritation of the eye or if the condition worsens or persists

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    • pull handle on the activating door to initiate flow
    • lower head into flow for 15 minutes
    • if necessary, continue flushing with emergency eyewash or shower
    • do not reuse
    • discard cartridge after use
  • Inactive ingredients

    benzlkonium chloride, edetate disodium, sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

  • Questions?

    Call 1-800-430-5490

    Sperian Eye & Face Protecton, Inc.

    (a Honeywell Company)

    825 East Highway 151

    Platteville, WI 53818 USA

  • Principle Display Panel

    Fendall 2000Fendall 2000 PI

  • INGREDIENTS AND APPEARANCE
    FENDALL 2000 PURE FLOW 
    purified water liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0631
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER98.6 L  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0631-3729.9 L in 1 CONTAINER; Type 0: Not a Combination Product12/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01812/15/2018
    Labeler - Honeywell Safety Products USA, Inc. (118768815)
    Establishment
    NameAddressID/FEIBusiness Operations
    Keystone Industries014769301manufacture(0498-0631)
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