Label: EYE WASH- purified water liquid

  • NDC Code(s): 68599-1981-1, 68599-1981-4
  • Packager: McKesson
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated June 10, 2021

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Drug Facts
    Active ingredient
    Purified water 98.3%

  • PURPOSE

    Purpose Eyewash

  • INDICATIONS & USAGE

    For external use only
    Do not use
    • if you experience any open wounds in or near the eyes and get medical help right away
    • 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

  • WARNINGS

    Warnings
    For external use only
    Do not use

    • if you experience any open wounds in or near the eyes and get medical help right away
    • if solution changes color or becomes cloudy

  • STOP USE

    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

    Keep out of reach of children.

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

  • DOSAGE & ADMINISTRATION

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

  • OTHER SAFETY INFORMATION

    Other information
    • for your protection, this bottle has an imprinted white seal with black printing “TAMPER EVIDENT SEAL”
    • do not use if this seal is missing or broken
    • use before expiration date marked on bottle
    • lot number is printed on the bottle
    • store at 20º to 25ºC (68º to 77ºF)

  • INACTIVE INGREDIENT

    Inactive ingredients
    boric acid, sodium borate, sodium chloride

  • QUESTIONS

    Questions? Call 1-800-777-4908

  • 1 fl oz

    NDC 68599-1981-1

    McKesson

    Eye Wash

    98.3% PURIFIED WATER
    OPHTHALMIC SOLUTION | STERILE

    MFR# MCK19828

    1 fl oz
    (29.6 mL)

    Distributed by
    McKesson Medical-Surgical Inc.
    Richmond, VA 23233
    PVN A0221
    Made in Canada


    1 fl oz eye wash solution
    Drug Facts
    Active ingredient Purpose
    Purified water 98.3% Eyewash
    Use
    For cleansing the eye to remove loose foreign material
    Warnings
    For external use only
    Do not use
    • if you experience any open wounds in or near the eyes and get medical help right away
    • 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 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
    Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle.
    Other information
    • for your protection, this bottle has an imprinted white seal with black printing “TAMPER EVIDENT SEAL”
    • do not use if this seal is missing or broken
    • use before expiration date marked on bottle
    • lot number is printed on the bottle
    • store at 20º to 25ºC (68º to 77ºF)
    Inactive ingredients
    boric acid, sodium borate, sodium chloride
    Questions? Call 1-800-777-4908

    28 each28 case

  • 4 fl oz

    68599-1981-4

    McKesson

    Eye Wash

    98.3% PURIFIED WATER
    OPHTHALMIC SOLUTION | STERILE

    MFR# MCK19818

    4fl oz

    (118.3mL)

    Distributed by
    McKesson Medical-Surgical Inc.
    Richmond, VA 23233
    PVN A0221
    Made in Canada


    4 fl oz eye wash solution
    Drug Facts
    Drug Facts
    Active ingredient Purpose
    Purified water 98.3% 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 you experience any open wounds in or near the eyes 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 experience
    • changes in vision
    • eye pain
    • condition worsens or persists
    • continued redness or irritation of the eye
    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
    • lot number is printed on the bottle
    • store at 20º to 25ºC (68º to 77ºF)
    • for your protection, this bottle has an imprinted white seal with black printing “TAMPER EVIDENT SEAL”
    • do not use if this seal is missing or broken
    • use before expiration date marked on bottle
    Inactive ingredients
    boric acid, sodium borate, sodium chloride
    Questions? Call 1-800-777-4908

    18 each18 case

  • INGREDIENTS AND APPEARANCE
    EYE WASH 
    purified water liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68599-1981
    Route of AdministrationIRRIGATION
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER98.3 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68599-1981-129.6 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product04/01/2021
    2NDC:68599-1981-4118.3 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product04/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02230504/01/2021
    Labeler - McKesson (023904428)
    Establishment
    NameAddressID/FEIBusiness Operations
    Niagara Pharmaceuticals205477792relabel(68599-1981) , repack(68599-1981) , manufacture(68599-1981)