Label: LUBRICANT EYE DROPS- propylene gycol 0.6% solution/ drops

  • NDC Code(s): 85185-002-10, 85185-002-20
  • Packager: Solis Pharmaceuticals Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 1, 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
    • for use as a protectant against further irritation or to relieve dryness of the eye
    • for use as a lubricant to prevent further irritation or to relieve dryness of the eye
  • 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

    Stop use and ask a doctor if

    you experience any of the following:

    • eye pain,
    • changes 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 a Poison Control Center right away.

  • Directions

    • shake well before using
    • Instill 1 or 2 drops in the affected eye(s) as needed.
  • Other information

    • store at room temperature
    • retain carton for future reference
  • Inactive ingredients

    benzalkonium chloride solution, boric acid, calcium chloride, castor oil, disodium edetate, magnesium chloride, polyoxyl 40 hydrogenated castor oil, potassium chloride, purified water, sodium borate, sodium chloride, sodium hyaluronate. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

  • PRINCIPAL DISPLAY PANEL

    Label

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    Twin Pack

  • INGREDIENTS AND APPEARANCE
    LUBRICANT EYE DROPS 
    propylene gycol 0.6% solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85185-002
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL6 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85185-002-101 in 1 CARTON03/01/2025
    110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:85185-002-202 in 1 CARTON03/01/2025
    210 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 DrugM01803/01/2021
    Labeler - Solis Pharmaceuticals Inc. (119380963)
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