Label: CHILDREN CLARITIN ALLERGY- loratadine solution

  • NDC Code(s): 11523-4360-1, 11523-4360-2, 11523-4360-3, 11523-4360-4, view more
    11523-4360-5, 11523-4360-6, 11523-4360-7
  • Packager: Bayer HealthCare LLC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated December 6, 2024

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  • Drug Facts

  • Active ingredient (in each 5 mL teaspoonful)

    Loratadine 5 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

    Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

  • ASK DOCTOR

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

  • WHEN USING

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

  • STOP USE

    Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • ASK DOCTOR/PHARMACIST

  • Directions

    Use only with enclosed dosing cup

    • adults and children 6 years and over: 2 teaspoonfuls (tsp) daily; do not take more than 2 teaspoonfuls (tsp) in 24 hours
    • children 2 to under 6 years of age: 1 teaspoonful (tsp) daily; do not take more than 1 teaspoonful (tsp) in 24 hours
    • children under 2 years of age: ask a doctor
    • consumers with liver or kidney disease: ask a doctor
  • OTHER SAFETY INFORMATION

    • each teaspoonful contains: sodium 6 mg
    • do not use if tape imprinted with “SEALED FOR YOUR PROTECTION” on top and bottom flaps of carton is not intact.
    • store between 20° and 25°C (68° and 77°F)
  • INACTIVE INGREDIENT

    edetate disodium, flavor, glycerin, maltitol, monobasic sodium phosphate, phosphoric acid, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose

  • Questions or comments?

    1-800-CLARITIN (1-800-252-7484) or www.claritin.com

  • PRINCIPAL DISPLAY PANEL

    4 oz. carton label

  • INGREDIENTS AND APPEARANCE
    CHILDREN CLARITIN  ALLERGY
    loratadine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-4360
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE5 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    MALTITOL (UNII: D65DG142WK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHOSPHORIC ACID (UNII: E4GA8884NN)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorGRAPEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11523-4360-51 in 1 CARTON05/26/2015
    1240 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:11523-4360-21 in 1 CARTON09/25/2015
    2120 mL in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:11523-4360-61 in 1 CARTON10/05/2015
    3180 mL in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:11523-4360-41 in 1 CARTON11/01/2015
    430 mL in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:11523-4360-72 in 1 CARTON03/01/2016
    5180 mL in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:11523-4360-31 in 1 CARTON01/01/2016
    6150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:11523-4360-11 in 1 CARTON05/26/2015
    760 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02064105/26/2015
    Labeler - Bayer HealthCare LLC. (112117283)
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