EYE WASH (PURIFIED WATER) LIQUID [PROVISION MEDICAL PRODUCTS]

EYE WASH (PURIFIED WATER) LIQUID [PROVISION MEDICAL PRODUCTS]
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NDC 69103-2180-7, 69103-2180-8
Set ID 0ebfbede-6345-4ed4-a817-49e0280d6db1
Category HUMAN OTC DRUG LABEL
Packager Provision Medical Products
Generic Name
Product Class
Product Number
Application Number PART349
  • INDICATIONS & USAGE

    Uses:

    fOR CLEANSING THE EYE TO HELP RELIEVE IRRITATION OR BURNING BY REMOVING LOOSE FOREIGN MATERIAL

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health

    professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. iF SWALLOWED, get medical help or

    contact a Poison Control Center right

    away.

  • WARNINGS

    Warnings:

    For external use only. 

    Do not use if: you experience any open wounds in or near the eye and obtain immediate medical treatment. 

    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

    Stop use and ask a doctor if you have any of the following:  Changes in vision.  Eye pain.  Condition worsens or persists.  Continued redness or irritation of the eye.

  • DOSAGE & ADMINISTRATION

    Directions:

    Flush the affacted eye as needed, controlling the rate of flow of solution by pressure on the bottle.

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    sodium chloride

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT-PURIFIED WATER 98.3%

  • PURPOSE

    EYEWASH

  • PRINCIPAL DISPLAY PANEL

    Provision 8 ounce bottle

  • INGREDIENTS AND APPEARANCE
    EYE WASH 
    purified water liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69103-2180
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER983 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69103-2180-8236 mL in 1 BOTTLE; Type 0: Not a Combination Product07/23/2015
    2NDC:69103-2180-7118 mL in 1 BOTTLE; Type 0: Not a Combination Product07/23/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34907/23/2015
    Labeler - Provision Medical Products (036936831)
    Registrant - Provision Medical Products (036936831)

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