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QUALITY CHOICE LUBRICANT EYE (CHAIN DRUG MARKETING ASSOCIATION INC)

Available Formats

Dosage Form Package Information Links
SOLUTION/ DROPS 1 BOTTLE in 1 CARTON (63868-968-15) > 15 mL in 1 BOTTLE Label Information

Complete QUALITY CHOICE LUBRICANT EYE Information

  • ACTIVE INGREDIENT

    Active ingredients                                                      Purpose

    Polyethylene Glycol 400 (0.4%)..................................Lubricant

    Propylene Glycol (0.3%).............................................Lubricant


  • PURPOSE

    Uses

    For the relief of burning, irritation due to dryness of the eye.


  • WARNINGS

    Warnings

    For external use only.


  • DO NOT USE

    Do not use

    • if solution changes color or becomes cloudy
    • if you are sensitive or allergic to any ingredient in this product

  • WHEN USING

    When using this product

    • to avoid contamination, do not touch tip of container to any surface
    • replace cap after each use

  • STOP USE

    Stop use and ask a doctor if

    • you experience eye pain
    • changes in vision occur
    • redness or irritation of the eye(s) gets worse or lasts 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, Calcium Chloride, Chlorhexidine Gluconate, Hydrochloric Acid, Hydroxypropyl Guar,

    Magnesium Chloride, Potassium Chloride, Purified Water, Sodium Chloride, Zinc Chloride


  • 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 LUBRICANT EYE  
    polyethylene glycol 400, propylene glycol solution/ drops
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-968
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 400 4 mg  in 1 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    BORIC ACID (UNII: R57ZHV85D4)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ZINC CHLORIDE (UNII: 86Q357L16B)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63868-968-15 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)