Label: ALLERGY RELIEF- loratadine tablet

  • NDC Code(s): 0363-1612-03, 0363-1612-46, 0363-1612-47, 0363-1612-60, view more
    0363-1612-65, 0363-1612-75, 0363-1612-88
  • Packager: Walgreen Company
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated March 30, 2022

If you are a healthcare professional or from the pharmaceutical industry 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

    ORIGINAL PRESCRIPTION STRENGTH

    Walgreens

    Compare to the active ingredient in Claritin® Tablets

    WALGREENS PHARMACIST RECOMMENDED

    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

    • 10 days of relief

    10 TABLETS

    ACTUAL SIZE

    *WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.

    612-94-allergy-relief
  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-1612
    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:0363-1612-4610 in 1 CARTON10/21/2021
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:0363-1612-471 in 1 CARTON10/21/2021
    2150 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:0363-1612-6020 in 1 CARTON10/21/2021
    31 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4NDC:0363-1612-651 in 1 CARTON10/21/2021
    430 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:0363-1612-751 in 1 CARTON12/07/2021
    590 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:0363-1612-881 in 1 CARTON03/08/2022
    6365 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:0363-1612-031 in 1 CARTON04/04/2022
    770 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07630110/21/2021
    Labeler - Walgreen Company (008965063)
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

More Info on this Drug

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