Label: CHILDRENS LORATADINE- loratadine tablet, chewable

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated June 28, 2024

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each chewable tablet)

    Loratadine USP, 5 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 useif you have ever had an allergic reaction to this product or any of its ingredients.

    Ask a doctor before use if you haveliver or kidney disease. Your doctor should determine if you need a different dose.

    When using this productdo not take more than directed. Taking more than directed may cause drowsiness.

    Stop use and ask a doctor ifan 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

    • chew or crush tablets completely before swallowing.

    adults and children 6 years and over

    chew 2 tablets daily; not more than 2 chewable tablets in 24 hours

    children 2 to under 6 years of age

    chew 1 tablet daily; not more than 1 chewable tablet in 24 hours

    children under 2 years of age

    ask a doctor

    consumers with liver or kidney disease

    ask a doctor

  • Other information

    • phenylketonurics: contains phenylalanine 1.25 mg per tablet.
    • TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
    • store between 20° to 25°C (68° to 77°F).
  • Inactive ingredients

    aspartame, carmine, citric acid anhydrous, colloidal silicon dioxide, flavor, magnesium stearate, mannitol, microcrystalline cellulose, sodium starch glycolate, stearic acid

  • Questions?

    Call 1-800-910-6874

  • SPL UNCLASSIFIED SECTION

    Distributed by Target Corporation
    Minneapolis, MN 55403

  • PRINCIPAL DISPLAY PANEL - 5 mg Tablet Blister Pack Carton

    NDC 11673-310-30

    Compare to active ingredient in Children's Claritin ® Chewables*

    Ages 2+ Years/ Dye-Free

    Children's Allergy

    Loratadine Chewable Tablets USP, 5 mg
    Antihistamine

    • Non-drowsy**
    • Indoor and outdoor allergies
    • 24-hour relief of sneezing, runny nose, itchy, watery eyes,itchy throat or nose

    up&up

    **When taken as directed. See drug facts panel.

    30 CHEWABLE TABLETS

    THE CHEWABLE TABLETS ARE
    TO BE CHEWED BEFORE SWALLOWING

    GRAPE
    FLAVOR

    ACTUAL SIZE

    30
    CHEWABLE
    TABLETS

    grape-target-spl

  • INGREDIENTS AND APPEARANCE
    CHILDRENS LORATADINE 
    loratadine tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-310
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE5 mg
    Inactive Ingredients
    Ingredient NameStrength
    ASPARTAME (UNII: Z0H242BBR1)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MANNITOL (UNII: 3OWL53L36A)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    Colorwhite (white to off-white) Scoreno score
    ShapeROUND (Flat face, beveled edge) Size10mm
    FlavorGRAPEImprint Code LC5
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-310-303 in 1 CARTON03/15/2024
    110 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21008803/15/2024
    Labeler - TARGET CORPORATION (006961700)
    Registrant - Ohm Laboratories (051565745)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ohm Laboratories184769029manufacture(11673-310)