Label: SHOPRITE ALLERGY RELIEF- loratadine tablet

  • NDC Code(s): 41190-612-46, 41190-612-72
  • Packager: Wakefern Food Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated 12/14

If you are a consumer or patient please visit this version.

  • Active ingredient (in each tablet)

    Loratadine 10 mg

    Close
  • Purpose

    Antihistamine

    Close
  • 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
    Close
  • 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. (1-800-222-1222)

    Close
  • 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

    Close
  • Other information

    do not use if blister unit is broken or torn {Blister Only}
    do not use if printed foil under cap is broken or missing {Bottle Only}
    store between 20° to 25°C (68° to 77°F)
    protect from excessive moisture {Blister Only}
    Close
  • Inactive ingredients

    lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

    Close
  • Questions or comments?

    1-800-SHOPRITE

    Close
  • Principal Display Panel

    Compare to: Active Ingredient in Claritin® Tablets

    NON-DROWSY†

    ORIGINAL PRESCRIPTION STRENGTH

    ALLERGY RELIEF

    Loratadine Tablets, 10 mg/Antihistamine

    INDOOR & OUTDOOR ALLERGIES

    24 Hour

    Relief of: Sneezing; Runny Nose; Itchy, Water Eyes; Itchy Throat or Nose

    actual size

    10 Days of Relief

    10 tablets

    †When taken as directed. See Drug Facts Panel.

    ShopRite Allergy Relief
    Close
  • INGREDIENTS AND APPEARANCE
    SHOPRITE ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:41190-612
    Route of Administration ORAL DEA Schedule     
    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)  
    POVIDONES (UNII: FZ989GH94E)  
    Product Characteristics
    Color WHITE Score no score
    Shape OVAL Size 8mm
    Flavor Imprint Code L612
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:41190-612-46 10 in 1 CARTON
    1 1 in 1 BLISTER PACK
    2 NDC:41190-612-72 1 in 1 CARTON
    2 60 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA076301 08/06/2013
    Labeler - Wakefern Food Corporation (069722418)
    Close