UP AND UP ALLERGY RELIEF (LORATADINE) TABLET [TARGET CORPORATION]

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UP AND UP ALLERGY RELIEF (LORATADINE) TABLET [TARGET CORPORATION]
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NDC 11673-612-03, 11673-612-46, 11673-612-58, 11673-612-65, 11673-612-72, 11673-612-76, 11673-612-78, 11673-612-82, 11673-612-87, 11673-612-95
Set ID c4ef0110-89c3-4ded-9a9a-75c0f794f869
Category HUMAN OTC DRUG LABEL
Packager Target Corporation
Generic Name
Product Class
Product Number
Application Number ANDA076301
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  • Active ingredient (in each tablet)

    Loratadine 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. (1-800-222-1222)

  • 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

    •
    do not use if printed foil under cap is broken or missing
    •
    store between 20° to 25°C (68° to 77°F)
  • Inactive ingredients

    lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

  • Questions?

    Call 1-888-547-7400

  • Principal Display Panel

    CE PACK

    Compare to active ingredient in Claritin®

    non-drowsy*

    allergy relief

    loratadine tablets, 10 mg

    antihistamine

    30 days of relief

    original prescription strength

    indoor and outdoor allergies

    24 hour relief of:

    sneezing

    runny nose

    itchy, watery eyes

    itchy throat or nose

    24 HOUR

    ACTUAL SIZE

    30 TABLETS

    30 TABLETS

    *When taken as directed. See drug facts panel.

    allergy relief image
  • INGREDIENTS AND APPEARANCE
    UP AND UP ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-612
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POVIDONE (UNII: FZ989GH94E)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize8mm
    FlavorImprint Code L612
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-612-4610 in 1 CARTON03/26/2012
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:11673-612-651 in 1 CARTON04/12/2012
    230 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:11673-612-721 in 1 CARTON04/16/201207/01/2016
    360 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:11673-612-761 in 1 CARTON04/12/201202/01/2016
    4120 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:11673-612-821 in 1 CARTON04/12/2012
    5200 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:11673-612-951 in 1 CARTON02/27/201302/27/2013
    645 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:11673-612-031 in 1 CARTON02/19/2015
    770 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:11673-612-78100 in 1 BOTTLE; Type 0: Not a Combination Product03/20/2015
    9NDC:11673-612-581 in 1 CARTON03/25/2015
    940 in 1 BOTTLE; Type 0: Not a Combination Product
    10NDC:11673-612-871 in 1 CARTON03/15/2016
    10300 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07630103/26/2012
    Labeler - Target Corporation (006961700)
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