Label: LORATADINE tablet, orally disintegrating

  • NDC Code(s): 51316-503-01, 51316-503-02, 51316-503-03, 51316-503-04, view more
    51316-503-05, 51316-503-06
  • Packager: CVS PHARMACY, INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated June 6, 2021

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • 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.

  • Directions

    • place 1 tablet on tongue; tablet disintegrates, with or without water
    adults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hours
    children under 6 years of ageask a doctor
    consumers with liver or kidney diseaseask a doctor

  • Other information

    • safety sealed: do not use if the individual blister unit imprinted with Loratadine Orally Disintegrating Tablet, USP is open or torn
    • store between 20° to 25°C (68° to 77°F)
    • use tablet immediately after opening individual blister
    • complies with USP Procedure 2 for Assay and Organic Impurities and Test 2 for Disintegration
  • Inactive ingredients

    anhydrous citric acid, mannitol, peppermint flavor, polysorbate 80, pullulan

  • Questions or comments?

    1-877-244-9825

  • SPL UNCLASSIFIED SECTION

    Manufactured by:

    Tenshi Kaizen Private Limited

    Bengaluru Rural – 562112, India

    Revised: 11/2020

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    CVS Health

    Indoor & Outdoor Allergies

    Children’s
    LORATADINE ORALLY
    DISINTEGRATING
    TABLETS USP, 10 mg

    Antihistamine

    Allergy Relief

    Non-Drowsy*

    Original Prescription Strength

    24 hour relief of:
    Sneezing; Runny nose; Itchy,
    watery eyes; Itchy throat or nose

    Ages 6 yrs & older
    30 ORALLY
    DISINTEGRATING
    TABLETS

    image

  • INGREDIENTS AND APPEARANCE
    LORATADINE 
    loratadine tablet, orally disintegrating
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-503
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    PULLULAN (UNII: 8ZQ0AYU1TT)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    MANNITOL (UNII: 3OWL53L36A)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize12mm
    FlavorMINTImprint Code T10
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51316-503-022 in 1 CARTON06/06/2021
    120 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:51316-503-033 in 1 CARTON06/06/2021
    230 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:51316-503-055 in 1 CARTON06/06/2021
    350 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4NDC:51316-503-066 in 1 CARTON06/06/2021
    460 in 1 BLISTER PACK; Type 0: Not a Combination Product
    5NDC:51316-503-044 in 1 CARTON06/06/2021
    540 in 1 BLISTER PACK; Type 0: Not a Combination Product
    6NDC:51316-503-011 in 1 CARTON06/06/2021
    610 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21329406/06/2021
    Labeler - CVS PHARMACY, INC (062312574)
    Establishment
    NameAddressID/FEIBusiness Operations
    Tenshi Kaizen Pvt Ltd675478488analysis(51316-503) , manufacture(51316-503) , pack(51316-503)