Label: ALLERGY RELIEF- loratadine tablet

  • NDC Code(s): 59779-612-03, 59779-612-39, 59779-612-46, 59779-612-49, view more
    59779-612-58, 59779-612-60, 59779-612-65, 59779-612-70, 59779-612-72, 59779-612-75, 59779-612-76, 59779-612-88, 59779-612-95
  • Packager: CVS Pharmacy
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated January 9, 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

    VALUE SIZE

    CVS Health

    Compare to the active ingredient in Claritin® Tablets

    Indoor & Outdoor Allergies

    Original Prescription Strength

    Non-Drowsy*

    24 HOUR

    Allergy Relief

    LORATADINE TABLETS, 10 mg

    Antihistamine

    24 hour relief of:

    Sneezing

    Itchy, watery eyes

    Runny nose

    Itchy throat or nose

    Actual Size

    365 TABLETS

    *When taken as directed.

    See Drug Facts Panel.

    612-17-allergy-relief
  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-612
    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:59779-612-4610 in 1 CARTON01/28/2009
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:59779-612-721 in 1 CARTON05/28/200908/31/2021
    260 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:59779-612-751 in 1 CARTON05/08/2009
    390 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:59779-612-581 in 1 CARTON07/26/200707/26/2007
    440 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:59779-612-3930 in 1 CARTON01/04/2005
    51 in 1 BLISTER PACK; Type 0: Not a Combination Product
    6NDC:59779-612-702 in 1 CARTON09/04/2015
    6NDC:59779-612-76120 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:59779-612-951 in 1 CARTON09/14/2015
    745 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:59779-612-4940 in 1 CARTON12/13/201509/30/2021
    81 in 1 BLISTER PACK; Type 0: Not a Combination Product
    9NDC:59779-612-031 in 1 CARTON10/10/2017
    970 in 1 BOTTLE; Type 0: Not a Combination Product
    10NDC:59779-612-88365 in 1 BOTTLE; Type 0: Not a Combination Product03/23/2018
    11NDC:59779-612-651 in 1 CARTON04/03/2018
    1130 in 1 BOTTLE; Type 0: Not a Combination Product
    12NDC:59779-612-6020 in 1 CARTON07/21/2009
    121 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07630101/04/2005
    Labeler - CVS Pharmacy (062312574)
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