Label: SODIUM CHLORIDE HYPERTONICITY- sodium chloride solution

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated September 20, 2024

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  • Active ingredient

    Sodium chloride 5%

  • 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
    ▪ if solution changes color or becomes cloudy

    When using this product
    ▪ it may cause temporary burning and irritation
    ▪ to avoid contamination do not touch tip of container to any surface
    ▪ replace cap after use

    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

    instill 1 or 2 drops in the affected eye(s) every 3 or 4 hours, or as directed by a physician.

    Other information

    ▪ store upright at 15°-25°C (59°-77°F)
    ▪ keep tightly closed
    ▪ serious side effects associated with use of the product may be reported to the phone number provided below

  • Inactive ingredients

    boric acid, hypromellose, propylene glycol, purified water, sodium borate. Hydrochloric acid and/or sodium hydroxide may be added to adjust pH. PRESERVATIVES ADDED: methylparaben 0.023%, propylparaben 0.01%.

    Questions

    [phone icon] Call 1-866-767-9161

  • Package/Label Principal Display Panel

    [heart icon] CVS
    Health ™

    Compare to the
    active ingredient
    in Muro 128 ®*
    NDC 69842-284-15

    Sodium
    Chloride
    Hypertonicity
    ophthalmic solution, 5%
    Temporary relief
    of corneal edema

    Actual Size Bottle
    on Side Panel

    STERILE

    15 mL (0.5 FL OZ)

    carton15mL
  • INGREDIENTS AND APPEARANCE
    SODIUM CHLORIDE HYPERTONICITY 
    sodium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-284
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-284-151 in 1 CARTON05/01/2021
    115 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01805/01/2020
    Labeler - CVS Pharmacy (062312574)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bausch & Lomb Incorporated079587625manufacture(69842-284)
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