Label: EYESALINE EMERGENCY EYEWASH- purified water liquid

  • NDC Code(s): 0498-0620-37
  • Packager: Honeywell Safety Products USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 5, 2024

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

  • 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

    Obtain immediate medical treatment for all open wounds in or near the eyes

    Do not use

    • if solution changes color or gets cloudy
    • with contact lenses
    • in open wounds in or near the eyes
    • if the eye is lacerated or object imbeded

    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

    remove contacts before using

    flush the affected area as needed

    if necessary continue flushing with emergency eyewash or shower

  • Other information

    • store at rom temperature, 59 o to 86 o F (15 o to 30 o C)
    • do not freeze
    • to avoid contamination, do not touch tip of container to any surface
    • once opened, discard
    • do not reuse
  • Inactive ingredients

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

  • Questions?

    1-800-430-5490

    Honeywell Safety Products USA, Inc. Smithfield, RI 02917

  • Principle Display Panel

    Emergency Eyewash PDP

  • Emergency Eyewash Directions

    Emergency EyewashDirections

  • INGREDIENTS AND APPEARANCE
    EYESALINE EMERGENCY EYEWASH 
    purified water liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0620
    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:0498-0620-373.78 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. (118768815)