Label: EYE DROPS- carboxymethylcellulose sodium liquid

  • NDC Code(s): 84938-001-01
  • Packager: Foshan Sugar Max Cosmetics CO.,Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 14, 2024

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  • SPL UNCLASSIFIED SECTION

    EYE DROPS

  • ACTIVE INGREDIENT

    Carboxymethylcellulose sodium 0.25%

  • PURPOSE

    Eye lubricant

  • INDICATIONS & USAGE

    Uses For the temporary relief of burning, irritation, anddiscomfort due to dryness of the eye or exposure towind or sun.
    May be used as a protectant against further irritation.

  • WARNINGS

    For external use only.
    To avoid contamination, do not touch tip of container toany surface. Replace cap after using.
    lf solution changes color or becomes cloudy, do not use.

  • STOP USE

    Stop use and ask a doctor if you experience eye pain,changes in vision, continued redness or irritation of theeye, or if the condition worsens or persists for more than72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. lf swallowed, get medicalhelp or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions Instilllor 2 drops in the affected eye(s) asneeded

  • STORAGE AND HANDLING

    Use only if tape seals on top and bottom flaps areintact.
    Use before expiration date marked on container.
    Discard 90 days after opening.

  • INACTIVE INGREDIENT

    calciumchloride
    Dequest
    magnesium chloride
    potassium chloride
    purified water
    sodium bicarbonate
    sodium chloride
    sodium perborate
    sodium phosphate

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    EYE DROPS 
    carboxymethylcellulose sodium liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84938-001
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED0.25 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CHLORIDE ANHYDROUS (UNII: OFM21057LP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PERBORATE (UNII: Y52BK1W96C)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    SODIUM PHOSPHATE (UNII: SE337SVY37)  
    AMINOTRIS(METHYLENEPHOSPHONIC ACID) (UNII: 1Y702GD0FG)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84938-001-012 in 1 BOX11/14/2024
    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 DrugM01811/14/2024
    Labeler - Foshan Sugar Max Cosmetics CO.,Ltd (700689935)
    Establishment
    NameAddressID/FEIBusiness Operations
    Foshan Sugar Max Cosmetics CO.,Ltd700689935manufacture(84938-001)
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