Label: BASE LABORATORIES CORNEAL FLOW HYPERTONICITY OPHTHALMIC EYE- sodium chloride ointment

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

Drug Label Information

Updated February 21, 2024

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  • Drug Facts

  • Active ingredient

    Sodium chloride 3%

    Purpose

    Hypertonicity agent

  • Uses:

    Temporary relief of corneal edema

  • Warnings:

    For external use only

    Do not use

    Except under the advice and supervision of a doctor

    When using this product

    • It may cause temporary burning and irritation 
    • Replace cap after use
    • To avoid contamination, do not touch top of container to any surface

    Stop use and ask a doctor if 

    • Condition worsens or persists for more than 72 hours
    • You experience eye pain, changes in vision, continued redness or irritation of the eye

    Keep out of reach of children.

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

  • Directions

    • Pull down the lower lid of the affected eye
    • Apply a small amount (1/4 inch) of ointment to the inside of eyelid
    • Apply every 3 to 4 hours or as directed by a doctor
  • Other information

    • Store at 15-25C (59-77F)
    • Keep tightly closed
    • Do not Freeze
    • Do not use if difficult to dispense or visible particles are seen in the product
    • Side effects associated with this product may be reported to the email address below
  • Inactive ingredients

    Water, Glycerin, Propylene Glycol, Squalane, Sodium Hyaluronate, Dimethicone, Tocopheryl Acetate, Carnosine, Butylene Glycol, Phenoxyethanol, Chlorphenesin, Ubiquinone

  • Questions or comments?

    cs@baselaboratories.com

  • Package Labeling:

    Label0

  • INGREDIENTS AND APPEARANCE
    BASE LABORATORIES CORNEAL FLOW HYPERTONICITY OPHTHALMIC EYE 
    sodium chloride ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80327-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE30 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SQUALANE (UNII: GW89575KF9)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARNOSINE (UNII: 8HO6PVN24W)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    UBIDECARENONE (UNII: EJ27X76M46)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80327-011-003 in 1 CARTON01/01/2023
    15 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01801/01/2023
    Labeler - Joonem LLC (117633878)
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