Label: EYE WASH- water solution

  • NDC Code(s): 50814-010-01
  • Packager: GFA Production (Xiamen) Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 9, 2024

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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 becomes cloudy

    When using this product

    • 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

    Keep out of reach of children.

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

    Stop use and ask a doctor if

    • you experience: • eye pain • changes in vision • continued redness • irritation of the eye • condition worsens or persists

  • 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° to 35°C (41° to 95°F)

  • Inactive ingredients

    Benzalkonium chloride, sodium chloride

  • Package Labeling:

    Eye wash

  • INGREDIENTS AND APPEARANCE
    EYE WASH 
    water solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50814-010
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER991 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50814-010-011 in 1 BOX08/09/201612/31/2025
    130 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/09/201612/31/2025
    Labeler - GFA Production (Xiamen) Co., Ltd. (421256261)
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