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Quality Choice Childrens Allergy Relief (Chain Drug Marketing Association Inc.)

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Dosage Form Package Information Links
SOLUTION 1 BOTTLE in 1 CARTON (63868-093-08) > 120 mL in 1 BOTTLE Label Information

Complete Quality Choice Childrens Allergy Relief Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredient (in each 5 mL teaspoonful)

    Cetirizine HCl 5 mg


  • Purpose

    Antihistamine


  • Uses

    temporarily relieves these symptoms due to hay fever or

    other upper respiratory allergies:

    • runny nose
    • itchy, watery eyes
    • sneezing
    • itching of the nose or throat

  • Warnings

    Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

    Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

    Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives.

    When using this product

    • drowsiness may occur
    • avoid alcoholic drinks
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery

    Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

    If pregnant or breast-feeding:

    • if breast-feeding: not recommended
    • if pregnant: ask a health professional before use.

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).


  • Directions

    • use only with enclosed dosing cup
    adults and children 6 years and over 1 teaspoonful (5 mL) or 2 teaspoonfuls (10 mL) once daily depending upon severity of symptoms; do not take more than 2 teaspoonfuls (10 mL) in 24 hours.
    adults 65 years and older 1 teaspoonful (5 mL) once daily; do not take more than 1 teaspoonful (5 mL) in 24 hours.
    children 2 to under 6 years of age ½ teaspoonful (2.5 mL) once daily. If needed, dose can be increased to a maximum of 1 teaspoonful (5 mL) once daily or ½ teaspoonful (2.5 mL) every 12 hours. Do not give more than 1 teaspoonful (5 mL) in 24 hours.
    children under 2 years of age ask a doctor
    consumers with liver or kidney disease ask a doctor

  • Other information

    • store between 20° to 25°C (68° to 77°F)

  • Inactive ingredients

    artificial grape flavor, glacial acetic acid, glycerin, methylparaben, natural and artificial banana flavor, propylene glycol, propylparaben, purified water, sodium acetate (anhydrous), sucralose


  • Questions?

    Call 248-449-9300


  • SPL UNCLASSIFIED SECTION

    Distributed by C.D.M.A., Inc.
    43157 W. Nine Mile
    Novi, MI 48376-0995


  • PRINCIPAL DISPLAY PANEL - 120 mL Bottle Carton

    QC
    QUALITY
    CHOICE
    ®

    NDC 63868-093-08

    Compare to the
    active ingredient in
    Children's ZYRTEC
    ®*

    children's
    Allergy
    Relief

    Cetirizine Hydrochloride
    Oral Solution, 1 mg/mL
    Antihistamine

    Indoor & Outdoor
    Allergies

    24 Hour Relief of:
    Runny Nose | Sneezing
    Itchy, watery eyes
    Itchy throat or nose

    2 Yrs. & older

    Sugar Free
    Grape
    Flavor

    Dosing Cup
    Included

    4 FL OZ (120 mL)

    Principal Display Panel - 120 mL Bottle Carton

  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE CHILDRENS ALLERGY RELIEF 
    cetirizine hydrochloride solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-093
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Cetirizine Hydrochloride (UNII: 64O047KTOA) (Cetirizine - UNII:YO7261ME24) Cetirizine Hydrochloride 1 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    acetic acid (UNII: Q40Q9N063P)  
    glycerin (UNII: PDC6A3C0OX)  
    methylparaben (UNII: A2I8C7HI9T)  
    propylene glycol (UNII: 6DC9Q167V3)  
    propylparaben (UNII: Z8IX2SC1OH)  
    water (UNII: 059QF0KO0R)  
    sodium acetate anhydrous (UNII: NVG71ZZ7P0)  
    sucralose (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    Color YELLOW (colorless to slightly yellow) Score     
    Shape Size
    Flavor GRAPE, BANANA Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63868-093-08 1 in 1 CARTON
    1 120 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA090182 09/08/2011
    Labeler - Chain Drug Marketing Association Inc. (011920774)
    Establishment
    Name Address ID/FEI Business Operations
    Taro Pharmaceutical Industries, Ltd. 600072078 MANUFACTURE(63868-093)
    Establishment
    Name Address ID/FEI Business Operations
    Taro Pharmaceuticals Inc. 206263295 MANUFACTURE(63868-093)