Home > Drugs A-Z > Quality Choice Cetirizine Hydrochloride

Quality Choice Cetirizine Hydrochloride (Chain Drug Marketing Association Inc.)

Available Formats

Dosage Form Package Information Links
TABLET 30 TABLET in 1 BOTTLE (63868-132-30) Label Information
TABLET 90 TABLET in 1 BOTTLE (63868-132-90) Label Information
TABLET 14 TABLET in 1 BLISTER PACK (63868-132-14) Label Information

Complete Quality Choice Cetirizine Hydrochloride Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredient (in each tablet)

    Cetirizine HCl, USP 10 mg


  • Purpose

    Antihistamine


  • Uses

    temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

    • runny nose
    • sneezing
    • itchy, watery eyes
    • 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

    adults and children 6 years and over one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms.
    adults 65 years and over ask a doctor
    children under 6 years of age ask a doctor
    consumers with liver or kidney disease ask a doctor

  • Other information

    • TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.
    • store between 20° to 25° C (68° to 77° F)

  • Inactive ingredients

    corn starch, hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol, povidone, talc, titanium dioxide


  • Questions?

    call 1-800-406-7984


  • SPL UNCLASSIFIED SECTION

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


  • PRINCIPAL DISPLAY PANEL - 10 mg Tablet Bottle Carton

    QUALITY®
    CHOICE

    NDC 63868-132-90

    †Compare to
    Active Ingredient in
    ZYRTEC®

    Original Prescription Strength

    All Day Allergy

    Cetirizine HCl Tablets, USP
    10 mg | Antihistamine

    Indoor & Outdoor Allergies

    24 Hour Relief of:
    Sneezing | Runny Nose
    Itchy, Watery Eyes | Itchy Throat or Nose

    90 Tablets 10 mg Each

    Principal Display Panel - 10 mg Tablet Bottle Carton

  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE CETIRIZINE HYDROCHLORIDE 
    cetirizine hydrochloride tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-132
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE 10 mg
    Inactive Ingredients
    Ingredient Name Strength
    STARCH, CORN (UNII: O8232NY3SJ)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Color white Score no score
    Shape RECTANGLE (rounded off) Size 9mm
    Flavor Imprint Code R152
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63868-132-14 14 in 1 BLISTER PACK; Type 0: Not a Combination Product 12/27/2007
    2 NDC:63868-132-30 30 in 1 BOTTLE; Type 0: Not a Combination Product 12/27/2007
    3 NDC:63868-132-90 90 in 1 BOTTLE; Type 0: Not a Combination Product 12/27/2007
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA077498 12/27/2007
    Labeler - Chain Drug Marketing Association Inc. (011920774)
    Registrant - Ranbaxy Pharmaceuticals Inc. (937890044)
    Establishment
    Name Address ID/FEI Business Operations
    Ohm Laboratories Inc. 184769029 manufacture(63868-132)