Label: OCTIQ LUBRICANT EYE DROPS- dextran 70 hypromellose solution/ drops

  • NDC Code(s): 57483-610-15
  • Packager: Innovus Pharmaceuticals, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 20, 2024

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  • Active ingredients

    Dextran 70 0.1%

    Hypromellose 2910 0.3%

  • Purpose

    Lubricant

    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
    • as a protectant against future irritation 
  • Warnings

    For external use only

  • Do not use

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

    • to avoid contamination, do not touch tip of container to any surface
    • replace cap after using 
  • Stop use and ask a doctor if

    • you feel eye pain
    • changes in vision occur redness or irritation of the eye gets worse or lasts more than 72 hours
  • Keep out of reach of children 

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

  • Directions

    • Put 1 or 2 drops in the affected eye(s) as needed
  • Other Information 

    • Store at room temperature
  • Inactive ingredients

    Boric acid, disodium edetate, potassium chloride, povidone, purified water, sodium borate, sodium chloride
    Preservative added: benzalkonium choride

  • Questions?

    Call 1.800.996.5122

    (Mon-Fri 9AM-5PM EST)

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    OCTIQ LUBRICANT EYE DROPS 
    dextran 70 hypromellose solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57483-610
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 701 mg  in 1 mL
    HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) (HYPROMELLOSE 2910 (4000 MPA.S) - UNII:RN3152OP35) HYPROMELLOSE 2910 (4000 MPA.S)3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    POVIDONE (UNII: FZ989GH94E)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57483-610-152 in 1 CARTON11/14/202110/31/2024
    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 DrugM11/14/202110/31/2024
    Labeler - Innovus Pharmaceuticals, Inc. (962507187)
    Establishment
    NameAddressID/FEIBusiness Operations
    AMMAN PHARMACEUTICAL INDUSTRIES534677849manufacture(57483-610)
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