Label: ALLERGY RELIEF- loratadine tablet

  • NDC Code(s): 11822-0612-1, 11822-0612-2, 11822-0612-3, 11822-0612-4, view more
    11822-0612-5, 11822-0612-6, 11822-0612-7, 11822-0612-8, 11822-0612-9
  • Packager: Rite Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated June 14, 2023

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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 or comments?

    1-800-719-9260

  • Principal Display Panel

    FREE FROM

    GLUTEN FREE

    24 HOUR

    Compare to the active ingredient of Claritin® Tablets

    ORIGINAL PRESCRIPTION STRENGTH

    ALLERGY RELIEF

    LORATADINE TABLETS, 10 mg

    ANTIHISTAMINE

    NON-DROWSY*

    INDOOR & OUTDOOR ALLERGIES

    24 HOUR RELIEF OF

    Sneezing • Runny nose

    Itchy, watery eyes

    Itchy throat or nose

    ACTUAL SIZE

    *WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.

    30 TABLETS

    allergy relief-image
  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0612
    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:11822-0612-21 in 1 CARTON10/21/2004
    110 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:11822-0612-13 in 1 CARTON11/18/2004
    210 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:11822-0612-31 in 1 CARTON07/08/2005
    360 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:11822-0612-41 in 1 CARTON04/15/2005
    4120 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:11822-0612-51 in 1 CARTON01/23/2014
    545 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:11822-0612-62 in 1 CARTON05/19/202005/19/2020
    610 in 1 BLISTER PACK; Type 0: Not a Combination Product
    7NDC:11822-0612-71 in 1 CARTON05/19/2020
    7300 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:11822-0612-81 in 1 CARTON04/25/2023
    870 in 1 BOTTLE; Type 0: Not a Combination Product
    9NDC:11822-0612-91 in 1 CARTON06/14/2023
    930 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07630110/21/2004
    Labeler - Rite Aid Corporation (014578892)
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