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FAMILY CARE LUBRICANT SINGLE USE EYE (UNITED EXCHANGE CORP)

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SOLUTION 5 VIAL, SINGLE-USE in 1 CARTON (65923-555-02) > .8 mL in 1 VIAL, SINGLE-USE Label Information

Complete FAMILY CARE LUBRICANT SINGLE USE EYE Information

  • ACTIVE INGREDIENT

    Active ingredient                                                                     Purpose

    Carboxymethylcellulose Sodium 0.5%......................................Eye Lubricant


  • PURPOSE

    Uses

    • For the temporary relief of burning and discomfort due to dryness of the eye or exposure to wind or sun
    • May be used as a protectant against further irritation

  • WARNINGS

    Warnings

    For external use only

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

    Do not reuse. Once opened, discard

    • Do not touch unit-dose tip of eye
    • if solution changes color or becomes cloudy, do not use



  • DO NOT USE

    Do not reuse. Once opened, discard

    • Do not touch unit-dose tip of eye
    • if 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 the eye, or if the condition worsens or persists for more than 72 hours


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


  • INDICATIONS & USAGE

    Directions

    To open, TWIST AND PULL TAB TO REMOVE.  Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

    • If used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor's instructions.

  • STORAGE AND HANDLING

    Other information

    • Use only if single-use container is intact.
    • Use before expiration date marked on container.
    • Store at 59° to 86°F (15° to 30°C)
    • RETAIN THIS CARTON FOR FUTURE REFERENCE.

  • INACTIVE INGREDIENT

    calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride, and sodium lactate.  May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.


  • DOSAGE & ADMINISTRATION

    Distributed by:

    UNITED EXCHANGE CORP.

    17211 Valley View Ave.

    Cerritos, CA 90703 USA

    MADE IN KOREA


  • INGREDIENTS AND APPEARANCE
    FAMILY CARE LUBRICANT SINGLE USE EYE 
    carboxymethylcellulose sodium solution/ drops
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:65923-555
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM 5 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:65923-555-02 5 in 1 CARTON 03/28/2013
    1 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part349 02/28/2013
    Labeler - UNITED EXCHANGE CORP (840130579)