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Medicine Shoppe Loratadine Allergy Relief (The Medicine Shoppe International)

Available Formats

Dosage Form Package Information Links
TABLET 90 TABLET in 1 BOTTLE (49614-170-75) Label Information
TABLET 30 TABLET in 1 BLISTER PACK (49614-170-65) Label Information

Complete Medicine Shoppe Loratadine Allergy Relief Information

  • ACTIVE INGREDIENT (IN EACH TABLET)

    Loratadine USP, 10 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.

    Ask a doctor before use if you have

    liver or kidney disease. Your doctor should determine if you need a different dose.

    When using this product

    do not take more than directed. Taking more than directed may cause drowsiness.

    Stop use and ask a doctor if

    an allergic reaction to this product occurs. Seek medical help right away.

    If pregnant or breast-feeding

    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.


  • DIRECTIONS

    adults and children 6 years and over: 1 tablet daily; not more than 1 tablet in 24 hours

    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 BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
    • TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.
    • store between 20 and 25° C (68 and 77° F)
    • protect from excessive moisture

  • INACTIVE INGREDIENTS

    corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch


  • QUESTIONS?

    call 1-800-406-7984

    Keep the carton. It contains important information.

    See end panel for expiration date.

    Distributed by

    Medicine Shoppe International, Inc.

    Earth City, MO 63045

    www.medicineshoppe.com

    1800-325-1397


  • PRINCIPAL DISPLAY PANEL

    The Medicine Shoppe®

    NDC 49614-170-75

    Non-Drowsy*

    Original Prescription Strength

    Loratadine Tablets USP, 10 mg

    Antihistamine

    Indoor & Outdoor Allergies

    24 Hour Allergy Relief

    Relief of:

    Sneezing

    Runny Nose

    Itchy, Watery Eyes

    Itchy Throat or Nose

    *When taken as directed. See Drug Facts Panel.

    90 TABLETS

    Compare to Claritin®active ingredient†

    †This product is not manufactured or distributed by Schering-Plough HealthCare Products, Inc., owner of the registered trademark Claritin®.

    This is the 90 count blister carton label for Loratadine Medicine Shoppe.
    This is the 90 count bottle carton label for Loratadine Medicine Shoppe.

  • INGREDIENTS AND APPEARANCE
    MEDICINE SHOPPE LORATADINE ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:49614-170
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    Color white (white to off white) Score no score
    Shape ROUND Size 6mm
    Flavor Imprint Code RX526
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49614-170-75 90 in 1 BOTTLE
    2 NDC:49614-170-65 30 in 1 BLISTER PACK
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA076134 08/19/2003
    Labeler - The Medicine Shoppe International (071997654)
    Registrant - Ranbaxy Pharmaceuticals Inc. (937890044)
    Establishment
    Name Address ID/FEI Business Operations
    Ohm Laboratories Inc. 051565745 manufacture