Label: FENDALL PURE FLOW- purified water liquid

  • NDC Code(s): 0498-0630-37
  • Packager: Honeywell Safety Products USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 10, 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

    Do not use

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

    Stop use and ask a doctor if you have

    • changes in vision
    • eye pain
    • continued redness or irritation of the eyes 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 activation 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
  • Other information

    • store at rom temperature, 59 o to 86 o F (15 o to 30 o C)
    • do not freeze
  • Inactive ingredients

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

  • Questions?

    USA: 800-430-5490 Canada: 888-212-7233

    Honeywell Safety Products USA, Inc.

    855 S. Mint Street, Charlotte, NC, 28202

  • Principle Display Panel

    32-005565 Rev. N - NDC 0498-0630-37

  • INGREDIENTS AND APPEARANCE
    FENDALL PURE FLOW 
    purified water liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0630
    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
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0630-3714.38 L in 1 CONTAINER; Type 0: Not a Combination Product12/15/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01812/15/2018
    Labeler - Honeywell Safety Products USA, Inc. (198541331)
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