Label: LORATADINE tablet

  • NDC Code(s): 59779-528-21, 59779-528-31, 59779-528-37, 59779-528-38, view more
    59779-528-43, 59779-528-56, 59779-528-60, 59779-528-69, 59779-528-93
  • Packager: CVS Pharmacy
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated December 21, 2021

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  • ACTIVE INGREDIENT (IN EACH TABLET)

    Loratadine, USP 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

    •
    store between 20° to 25° C (68° to 77° F)
    •
    protect from excessive moisture
    •
    TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.
  • INACTIVE INGREDIENTS

    Corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

  • QUESTIONS?

    Call 1-800-406-7984

  • PRINCIPAL DISPLAY PANEL - 10 mg Tablet Bottle Carton

    CVSHealth™

    Compare to the active
    ingredient in Claritin®†

    Indoor & Outdoor Allergies

    Original Prescription Strength

    Non-Drowsy*

    Allergy Relief

    LORATADINE TABLETS, USP 10 mg
    Antihistamine

    24 Hour Relief of:

    1.
    Sneezing
    2.
    Runny nose
    3.
    Itchy, watery eyes
    4.
    Itchy throat or nose

    24
    HOUR

    Actual Bottle Size on Side Panel
    Package Contains One Bottle

    45 TABLETS

    Actual Size

    *When taken as directed.
    See Drug Facts Panel.

    Principal Display Panel - 10 mg Tablet Bottle Carton
  • INGREDIENTS AND APPEARANCE
    LORATADINE 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-528
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    Colorwhite (White to Off-White) Scoreno score
    ShapeROUNDSize6mm
    FlavorImprint Code RX526
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-528-561 in 1 CARTON01/08/2010
    15 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:59779-528-691 in 1 CARTON01/08/2010
    210 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:59779-528-212 in 1 CARTON01/08/2010
    310 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4NDC:59779-528-313 in 1 CARTON01/08/2010
    410 in 1 BLISTER PACK; Type 0: Not a Combination Product
    5NDC:59779-528-431 in 1 CARTON01/08/2010
    545 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:59779-528-372 in 1 CARTON01/08/2010
    6120 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:59779-528-381 in 1 CARTON01/08/2010
    7365 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:59779-528-601 in 1 CARTON01/08/2010
    860 in 1 BOTTLE; Type 0: Not a Combination Product
    9NDC:59779-528-932 in 1 CARTON01/08/2010
    930 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07613401/08/2010
    Labeler - CVS Pharmacy (062312574)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ohm Laboratories Inc.051565745MANUFACTURE(59779-528)
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