Label: WALGREENS SODIUM CHLORIDE OPHTHALMIC 5 PERCENT HYPERTONICITY EYE- sodium chloride ointment

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

Drug Label Information

Updated December 30, 2024

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  • SPL UNCLASSIFIED SECTION

    Walgreens Sodium Chloride Ophthalmic

    Ointment 5% Hypertonicity Eye Ointment 3.5g

    NDC 0363-7500-50

    Drug Facts

  • Active ingredient

    Sodium Chloride, 50 mg (5%)

  • Purpose

    Hypertonicity Agent

  • Use

    • For the temporary relief of corneal edema.

  • Warnings

    • For use in the eyesonly.

    • Retain outer carton for full product drug facts.

    Do not use

    this product except under the advice and supervision of a doctor.

    When using this product

    • avoid contamination, do not touch tip of container to any surface.

    • replace cap after use.

    • this product may cause temporary burning and irritation on being instilled into the eye.

    Stop use and ask a doctorif

    • you experience eye pain, changes in vision, continued redness or irritation of the eye.

    • condition worsens or persists for more than 72 hours.

    KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN.

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

  • Directions

    • pull down lower lid of the affected eye(s) and apply a small amount (1/4 inch) to the inside of the eyelid and apply every 3-4 hours, or as directed by a doctor.

  • Other information

    • Store at room temperature 15°- 30°C (59°- 86°F).

    • Do not freeze.

    • Keep tightly closed.

    • See crimp of tube or box for lot number and expiration date.

  • Inactive ingredients

    lanolin alcohol, mineral oil, water for injection and white petrolatum.

  • Questionsor comments?

    •1- 800-925-4733

  • PRINCIPAL DISPLAY PANEL

    NDC 0363-7500-50

    Sodium Chloride

    Ophthalmic

    Ointment, 5%

    Hypertonicity

    Eye Ointment

    NET WT 0.125 OZ (3.5 g)

    Carton

    Label

  • INGREDIENTS AND APPEARANCE
    WALGREENS SODIUM CHLORIDE OPHTHALMIC 5 PERCENT HYPERTONICITY EYE 
    sodium chloride ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7500
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP)  
    WATER (UNII: 059QF0KO0R)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-7500-501 in 1 CARTON04/01/2019
    13.5 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01804/01/2019
    Labeler - Walgreen Company (008965063)
    Registrant - KC Pharmaceuticals, Inc. (174450460)
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