Label: GOOD NEIGHBOR PHARMACY LORATADINE- loratadine tablet

  • NDC Code(s): 24385-471-12, 24385-471-52, 24385-471-58, 24385-471-65, view more
    24385-471-76, 24385-471-78, 24385-471-99
  • Packager: Amerisource Bergen
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated November 25, 2019

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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 blister unit is broken or torn {Blister Only}
    •
    do not use if printed foil under cap is broken or missing {Bottle Only}
    •
    store between 20° to 25°C (68° to 77°F)
    •
    protect from excessive moisture {Blister Only}
  • Inactive ingredients

    lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

  • Questions or comments?

    1-800-719-9260

  • Principal Display Panel

    Compare to Claritin® Tablets active ingredient

    Original Prescription Strength

    Loratadine tablets, 10 mg

    Antihistamine

    Indoor & Outdoor Allergies

    24 HOUR

    Relief of:

    Sneezing

    Runny Nose

    Itchy, Water Eyes

    Itchy Throat or Nose

    *When taken as direction.

    See Drug Facts Panel.

    Non-Drowsy*

    actual size

    10 Tablets

    Good Neighbor Pharmacy Loratadine Tablets
  • INGREDIENTS AND APPEARANCE
    GOOD NEIGHBOR PHARMACY LORATADINE 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-471
    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:24385-471-6530 in 1 CARTON12/02/2008
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:24385-471-5210 in 1 CARTON12/02/2008
    21 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:24385-471-781 in 1 CARTON11/10/2008
    390 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:24385-471-761 in 1 CARTON08/25/2014
    4120 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:24385-471-581 in 1 CARTON09/22/2011
    540 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:24385-471-991 in 1 CARTON09/22/2011
    630 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:24385-471-121 in 1 POUCH; Type 0: Not a Combination Product07/16/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07630111/10/2008
    Labeler - Amerisource Bergen (007914906)
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