Label: LUBRICANT EYE DROP- propylene glycol liquid

  • NDC Code(s): 71800-031-03, 71800-031-06
  • Packager: Innovida Pharmaeutique Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 18, 2025

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  • Active Ingredient

    Propylene Glycol 0.6%

  • Purpose

    Lubricant

  • Uses

    • for the temporary relief of burning and irritation due to dryness of the eye
    • for the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun
  • Warnings

    For external use only

    Do not use 

    • if this product changes color or becomes cloudy
    • if you are sensitive to any ingredient in this product

    When using this product

    •  do not touch tip of container to any surface to avoid contamination
    • replace cap after each use
    • remove contact lenses before use

    Stop use and ask a doctor if you experience any of the following:

    • Eye pain
    • change in vision
    • continued redness or irritation of the eye
    • condition worsens or persists for more than 72 hours
  • Keep out of reach of children

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

  • Directions

    Shake well before using. Put 1 or 2 drops in the affected eye (s) as needed

  • Other information

    store at room temperature

  • Inactive Ingredients

    Water, Boric Acid, Potassium Chloride, Sorbitol, Glycerin, Hyluronic Acid, Amynomethylpropanol, Benzalhonium Chloride, Sodium Chorlide, Hydrochloric Acid, Sodium Hydroxide

  • Product label

    image description

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  • INGREDIENTS AND APPEARANCE
    LUBRICANT EYE DROP 
    propylene glycol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71800-031
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BORIC ACID (UNII: R57ZHV85D4)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    SORBITOL (UNII: 506T60A25R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71800-031-031 in 1 BOX02/11/2025
    17.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:71800-031-062 in 1 BOX02/11/2025
    215 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01802/11/2025
    Labeler - Innovida Pharmaeutique Corporation (080892908)
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