Label: VIS GUARD LUBRICANT EYE DROPS- polyvinyl alcohol 1.4% solution/ drops

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 27, 2024

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

  • Active ingredient

    ​Polyvinyl alcohol 1.4%

  • Purpose

    Lubricant

  • Uses

    For the temporary relief of burning and irritation due to dryness of the eye.

  • Warnings

    For external use only

    Do not use this product

    If you are allergic to polyvinyl alcohol or any of the other listed ingredients.
    If solution changes color or becomes cloudy.
    While wearing contact lenses.

    When using this product

    Do not touch tip of container to your eye or to any surface to avoid contamination.
    Replace cap after each use.

    Stop use and ask a doctor if

    If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours, discontinue use and consult a doctor.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

  • Directions

    Instill 1 to 2 drops in the affected eye(s) as needed.

  • Other information

    Store at 15°-30°C (59°-86°F).
    Keep tightly closed.

  • Inactive ingredients

    benzalkonium chloride, dibasic sodium phosphate hydrate, disodium edetate hydrate, monobasic sodium phosphate dihydrate, sodium chloride, water for injection

  • DOSAGE & ADMINISTRATION

  • INDICATIONS & USAGE

  • ULAI HEALTH Vis Guard POLYVINYL ALCOHOL 1.4% LUBRICANT EYE DROPS 15ML

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  • INGREDIENTS AND APPEARANCE
    VIS GUARD LUBRICANT EYE DROPS 
    polyvinyl alcohol 1.4% solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73057-530
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990) POLYVINYL ALCOHOL, UNSPECIFIED1.4 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)  
    SODIUM PHOSPHATE, DIBASIC, DODECAHYDRATE (UNII: E1W4N241FO)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73057-530-081 in 1 BOX01/31/2024
    115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01801/31/2024
    Labeler - Ulai Health LLC (081181535)