Label: EYESALINE EMERGENCY EYEWASH- purified water liquid

  • NDC Code(s): 0498-0100-01, 0498-0100-02, 0498-0100-03, 0498-0100-04, view more
    0498-0100-05
  • Packager: Honeywell Safety Products USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 4, 2024

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  • Active ingredient

    Sterile Water 99%

  • Purpose

    Eyewash

  • Uses

    • for flushing the eye to remove loose foreign material, air pollutants or chlorinated water
  • Warnings

    For external use only- Obtain immediate medical treatment for all open wounds in or near eyes. To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.

    Do not use

    • if solution changes color or becomes cloudy
    • if you have open wounds in or near the eyes, get medical help right away.

    Stop use and ask a doctor if

    • you experience eye pain
    • changes in vision
    • continued redness or irritation of the eye
    • 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
    • twist top to remove
    • flush the affected area as needed
    • control rate of flow by pressure on the bottle
    • if necessary, continue flushing with emergency eyewash or shower

  • Inactive Ingredients

    sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

  • Questions?

    Call 1-800-430-5490

    Honeywell Safety Products USA, Inc. Smithfield, RI 02917

  • Sterile Eyewash Package label

    eyewash

  • INGREDIENTS AND APPEARANCE
    EYESALINE EMERGENCY EYEWASH 
    purified water liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0100
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER98.6 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0100-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product12/15/2018
    2NDC:0498-0100-02118 mL in 1 BOTTLE; Type 0: Not a Combination Product12/15/2018
    3NDC:0498-0100-03237 mL in 1 BOTTLE; Type 0: Not a Combination Product12/15/2018
    4NDC:0498-0100-04473 mL in 1 BOTTLE; Type 0: Not a Combination Product12/15/2018
    5NDC:0498-0100-05946 mL in 1 BOTTLE; 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)
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