Label: WALGREENS LUBRICANT EYE DROPS PRESERVATIVE FREE- dextran 70, hypromellose liquid

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

Drug Label Information

Updated December 20, 2023

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  • Active ingredients

    Dextran 70 0.1%

    Hypromellose 0.3%

  • Purposes

    Lubricant

    Lubricant

  • Use

    • temporary relief of discomfort due to dryness of the eye or to exposure to wind or sun
  • Warnings

    For external use only

    Do not use

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

    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 feel eye pain
    • changes in vision occur
    • redness or irritation of the eye(s) gets worse or lasts more than 72 hours

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

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

  • Directions

    • put 1 or 2 drops in the affected eye(s) as needed
  • Other information

    store at 15°-25°C (59°-77°F)

  • Inactive ingredients

    boric acid, disodium edetate hydrate, potassium chloride, purified water, sodium borate, sodium chloride

  • Questions or comments?

    Call 1-888-527-4276

  • Walgreens Lubricant Eye Drops Preservative Free 35ct

    Walgreens Lubricant Eye Drops Preservative Free 35ct

  • INGREDIENTS AND APPEARANCE
    WALGREENS LUBRICANT EYE DROPS PRESERVATIVE FREE 
    dextran 70, hypromellose liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0646
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 700.1 g  in 100 mL
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) (HYPROMELLOSE, UNSPECIFIED - UNII:3NXW29V3WO) HYPROMELLOSE, UNSPECIFIED0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BORIC ACID (UNII: R57ZHV85D4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0646-0135 in 1 BOX01/01/2020
    10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01801/01/2020
    Labeler - Walgreen Company (008965063)
    Registrant - KC Pharmaceuticals, Inc. (174450460)
    Establishment
    NameAddressID/FEIBusiness Operations
    KC Pharmaceuticals, Inc.174450460pack(0363-0646) , label(0363-0646)
    Establishment
    NameAddressID/FEIBusiness Operations
    Unimed689852052manufacture(0363-0646)
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