Label: EYE WASH- water liquid

  • NDC Code(s): 82996-007-01, 82996-007-02
  • Packager: Hubei Changjian Medical Products Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 20, 2023

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  • Drug Facts

  • Active ingredient

    Purified Water 99.1%

    Purpose

    Eyewash

  • Use

    • For cleansing the eye to help relieve irritation or burning by removing loose foreign material
  • Warnings

    For external use only

    Do not use

    if solution changes color or become cloudy

    When using this products

    • to avoid contamination,do not touch tip of container to any surface do not reuse
    • once opened, discard
    • obtain immediate medical treatment
    • for all open wounds in or near the eyes 

    Stop use and ask a doctor if

    • eye pain
    • changes in vision
    • continued redness
    • 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

    • Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle 
  • Other information:

    • not for use as contact lens solution
    • Use before expiration date marked on the bottle
    • Store at room temperature,5°C to 35°C
  • lnactive ingredients

    sodium chloride

  • SPL UNCLASSIFIED SECTION

    To report a serious adverse event. contact +1 (855)924-2182

  • Package Labeling: 82996-007-01

    Label2

  • Package labeling: 82996-007-02

    Label 30mL

  • INGREDIENTS AND APPEARANCE
    EYE WASH 
    water liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82996-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER991 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82996-007-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product09/20/2023
    2NDC:82996-007-0230 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01809/20/2023
    Labeler - Hubei Changjian Medical Products Co., Ltd. (699440035)
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