Label: ALLERGY RELIEF- loratadine tablet

  • NDC Code(s): 30142-612-03, 30142-612-46, 30142-612-58, 30142-612-65, view more
    30142-612-72, 30142-612-76, 30142-612-88, 30142-612-92
  • Packager: Kroger Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated May 12, 2020

If you are a consumer or patient 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?

    1-800-632-6900

  • Principal Display Panel

    COMPARE TO the active ingredient of CLARITIN® TABLETS

    See back panel

    BIG DEAL! 365 TABLETS

    OUR PHARMACIST RECOMMENDED

    ORIGINAL PRESCRIPTION STRENGTH

    NON-DROWSY*

    365 Days Of Relief

    Allergy Relief

    Loratadine Tablets 10 mg

    Antihistamine

    INDOOR & OUTDOOR ALLERGIES

    actual size

    24 HOUR RELIEF OF:

    Sneezing

    Runny Nose

    Itchy, Watery Eyes

    Itchy Throat or Nose

    24 HOUR

    365 TABLETS

    Contains 1 Bottle with 365 Tablets

    *When taken as directed.

    See Drug Facts Panel.

    allergy relief image
  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-612
    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, UNSPECIFIED (UNII: FZ989GH94E)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize8mm
    FlavorImprint Code L612
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30142-612-4610 in 1 CARTON10/08/2005
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:30142-612-651 in 1 CARTON10/13/2005
    230 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:30142-612-721 in 1 CARTON02/04/200608/10/2015
    360 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:30142-612-761 in 1 CARTON08/22/200507/17/2019
    4120 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:30142-612-031 in 1 CARTON03/19/2014
    570 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:30142-612-581 in 1 CARTON04/05/2014
    640 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:30142-612-922 in 1 CARTON01/16/2018
    770 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:30142-612-881 in 1 CARTON04/19/2018
    8365 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07630108/22/2005
    Labeler - Kroger Company (006999528)