Label: WAL-ITIN- loratadine tablet

  • NDC Code(s): 0363-9150-03, 0363-9150-05, 0363-9150-10, 0363-9150-15, view more
    0363-9150-20, 0363-9150-30, 0363-9150-45, 0363-9150-65, 0363-9150-70, 0363-9150-90
  • Packager: Walgreens
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated May 11, 2022

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

  • 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
    • sneezing
    • itchy, watery eyes
    • 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 (1-800-222-1222) right away.

  • Directions

    adults and children 6 years and over1 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 20º-25ºC (68º-77ºF) (see UPS Controlled Room Temperature)
    • protect from light
  • Inactive ingredients

    lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

  • Questions or comments?

    Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

  • Principal Display Panel

    Compare to the active ingredient in Claritin®  24 Hour††

    NON-DROWSY* 

    Allergy Relief

    24 HOUR ALLERGY

    LORATADINE TABLETS, 10 mg / ANTIHISTAMINE

    24 HOUR  Indoor & Outdoor Allergies

    • Relief of sneezing; runny nose; itchy, watery eyes & Itchy throat or nose
    • 365 days of relief

    *WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.

    TABLETS

    Gluten Free

    †This product is not manufactured or distributed by Bayer Healthcare LLC, distributor of Claritin® 24 Hour.

    TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

    KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

    DISTRIBUTED BY: WALGREEN CO.

    200 WILMOT RD., DEERFIELD, IL 60015

    walgreens.com


  • Package Label

    Loratadine, USP 10 mg

    WALGREENS Non-Drowsy Allergy Relief

  • INGREDIENTS AND APPEARANCE
    WAL-ITIN 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9150
    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)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize6mm
    FlavorImprint Code 439
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-9150-1010 in 1 CARTON12/27/2019
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:0363-9150-2020 in 1 CARTON12/27/2019
    21 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:0363-9150-055 in 1 CARTON12/27/2019
    31 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4NDC:0363-9150-301 in 1 BOX12/27/2019
    4300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    5NDC:0363-9150-151 in 1 CARTON12/27/2019
    5150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    6NDC:0363-9150-901 in 1 BOX12/27/2019
    690 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    7NDC:0363-9150-701 in 1 BOX12/27/2019
    770 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    8NDC:0363-9150-451 in 1 BOX12/27/2019
    845 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    9NDC:0363-9150-031 in 1 BOX12/27/2019
    930 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    10NDC:0363-9150-651 in 1 BOX12/27/2019
    10365 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07520912/27/2019
    Labeler - Walgreens (008965063)