Label: GOOD SENSE ALLERGY RELIEF- loratadine tablet

  • NDC Code(s): 0113-0612-39, 0113-0612-46, 0113-0612-49, 0113-0612-58, view more
    0113-0612-60, 0113-0612-65, 0113-0612-75, 0113-0612-88
  • Packager: L. Perrigo Company
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 15, 2022

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • 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 or comments?

    1-800-719-9260

  • Principal Display Panel

    Non-Drowsy*

    *When taken as directed. See Drug Facts Panel.

    Original Prescription Strength

    Allergy Relief

    Loratadine Tablets, 10 mg

    Antihistamine

    Actual Size

    Indoor & Outdoor Allergies

    24 Hour Relief of:

    Sneezing

    Runny Nose

    Itchy, Watery Eyes

    Itchy Throat or Nose

    90 Tablets

    Compare to active ingredient of Claritin® Tablets

    100% SATISFACTION GUARANTEED

    612C2-allergy-relief
  • INGREDIENTS AND APPEARANCE
    GOOD SENSE ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0113-0612
    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, UNSPECIFIED (UNII: FZ989GH94E)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize8mm
    FlavorImprint Code L612
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0113-0612-3930 in 1 CARTON11/28/2005
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:0113-0612-4610 in 1 CARTON09/21/2004
    21 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:0113-0612-6020 in 1 CARTON09/21/2004
    31 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4NDC:0113-0612-651 in 1 CARTON10/06/2004
    430 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:0113-0612-4940 in 1 CARTON05/28/201312/31/2019
    51 in 1 BLISTER PACK; Type 0: Not a Combination Product
    6NDC:0113-0612-881 in 1 CARTON09/21/2004
    6365 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:0113-0612-581 in 1 CARTON09/21/200409/21/2004
    740 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:0113-0612-751 in 1 CARTON06/06/2020
    890 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07630109/21/2004
    Labeler - L. Perrigo Company (006013346)