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QUALITY CHOICE LUBRICATING EYE DROPS (CHAIN DRUG MARKETING ASSOCIATION INC)

Available Formats

Dosage Form Package Information Links
SOLUTION 1 BOTTLE in 1 CARTON (63868-969-15) > 15 mL in 1 BOTTLE Label Information

Complete QUALITY CHOICE LUBRICATING EYE DROPS Information

  • ACTIVE INGREDIENT

    Active ingredients------------------------------------------------Purpose

    Carboxymethylcellulose Sodium 0.5%-------------------Lubricant

    Glycerin 0.9%-----------------------------------------------------Lubricant


  • PURPOSE

    Uses

    • For the temporary relief of burning, irritation and discomfort due to dryness of the eye or from irritation from wind or sun.

  • WARNINGS

    Warnings

    • For external use only

  • WHEN USING


    When using this product

    • To avoid contamination, do not touch tip of container to any surface.  Replace cap after using.
    • Do not use if solution changes color or gets cloudy.


  • STOP USE

    Stop use and ask a doctor if

    You feel 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 reach of children.

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


  • INDICATIONS & USAGE

    Directions

    Put 1 or 2 drops in the affected eye/s as needed.


  • STORAGE AND HANDLING

    Other information

    • some users may experience a brief tingling sensation
    • Store at room temperature.

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Boric Acid, Sodium Borate, Levocarnitin, Potassium Chloride, Calcium Chloride Dihydrate, Magnesium Chloride, Erythritol, Sodium Citrate Dihydrate, Potassium Sorbate, Purified Water


  • DOSAGE & ADMINISTRATION

    Distributed by C.D.M.A., Inc.

    43157 W. Nine Mile

    Novi, MI 48376-0995

    www.qualitychoice.com

    Made in Korea


  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE LUBRICATING EYE DROPS 
    carboxymethylcellulose sodium, glycerin solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-969
    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
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 9 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    BORIC ACID (UNII: R57ZHV85D4)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    LEVOCARNITINE (UNII: 0G389FZZ9M)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    ERYTHRITOL (UNII: RA96B954X6)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63868-969-15 1 in 1 CARTON
    1 15 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part349 09/30/2012
    Labeler - CHAIN DRUG MARKETING ASSOCIATION INC (011920774)