Label: GOOD NEIGHBOR PHARMACY LORATADINE- loratadine tablet

  • NDC Code(s): 24385-471-12, 24385-471-52, 24385-471-58, 24385-471-61, view more
    24385-471-65, 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 December 11, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • 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
    •
    store between 20° to 25°C (68° to 77°F)
    •
    protect from excessive moisture
  • Inactive ingredients

    lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

  • Questions or comments?

    1-800-719-9260

  • Principal Display Panel

    GOOD NEIGHBOR PHARMACY®

    Compare to Claritin® Tablets active ingredient

    Original Prescription Strength

    NON-DROWSY*

    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 directed. See Drug Facts Panel.

    actual size

    10 Tablets

    GOOD NEIGHBOR PHARMACY LORATADINE CARTON IMAGE 1 OF 2
    GOOD NEIGHBOR PHARMACY LORATADINE CARTON IMAGE 2 OF 2
  • 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 CARTON12/02/200805/06/2013
    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 CARTON08/25/201412/24/2015
    4120 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:24385-471-581 in 1 CARTON09/22/201105/01/2017
    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 Product07/16/201407/16/2014
    8NDC:24385-471-611 in 1 CARTON12/11/2024
    8100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07630111/10/2008
    Labeler - Amerisource Bergen (007914906)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!