Label: AMAZON BASIC CARE ALLERGY RELIEF- loratadine tablet

  • NDC Code(s): 72288-452-09, 72288-452-19, 72288-452-30, 72288-452-36
  • Packager: Amazon.com Services LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated May 10, 2024

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  • Drug Facts

  • 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                                                                    
    • 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 (1-800-222-1222) right away.

  • 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


    • Tamper-evident: do not use if foil seal under cap, printed with “SEALED for YOUR PROTECTION” is missing, open or broken
    • store at 20° to 25°C (68° to 77°F)
    • protect from excessive moisture
  • Inactive ingredients

    lactose monohydrate, magnesium stearate, pregelatinized starch (maize), sodium starch glycolate.

  • Questions or comments?


    call 1-855-274-4122

    DISTRIBUTED BY:
    AMAZON.COM SERVICES LLC
    410 TERRY AVENUE N.,
    SEATTLE, WA 98109

    © 2024 AMAZON.COM , INC. OR ITS
    AFFILIATES. ALL RIGHTS RESERVED.

    Made in India



  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30 Tablets Container Label)

    amazon

    basic+care

    NDC 72288-452-09

    Allergy Relief

    Loratadine Tablets USP 10 mg
    Antihistamine

    Indoor & Outdoor Allergies
    Non-Drowsy*

    24 Hour Relief of: • Sneezing • Runny Nose
    • Itchy, Watery Eyes • Itchy Throat or Nose

    30 TABLETS

    *When taken as directed. See Drug Facts Panel.
    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30 Tablets Container Label)

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30 Tablets Container Carton)

    amazon

    basic+care

    Indoor & Outdoor Allergies
    NDC 72288-452-09

    Compare to
    Claritin®
    active ingredient**

    Allergy Relief

    Loratadine Tablets USP 10 mg |  Antihistamine
    Non-Drowsy*

    24 Hour Relief of:
    • Sneezing • Runny Nose
    • Itchy, Watery Eyes • Itchy Throat or Nose

    30 TABLETS                 

    *When taken as directed. See Drug Facts Panel.
    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30 Tablets Container Carton)

  • INGREDIENTS AND APPEARANCE
    AMAZON BASIC CARE ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72288-452
    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)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    Product Characteristics
    ColorWHITE (White to Off-white) Scoreno score
    ShapeROUNDSize6mm
    FlavorImprint Code 39;L
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72288-452-091 in 1 CARTON05/15/2024
    130 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:72288-452-191 in 1 CARTON05/15/2024
    290 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:72288-452-301 in 1 CARTON05/15/2024
    3300 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:72288-452-361 in 1 CARTON05/15/2024
    4365 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20831405/15/2024
    Labeler - Amazon.com Services LLC (128990418)
    Registrant - Aurohealth LLC (078728447)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aurobindo Pharma Limited650381903ANALYSIS(72288-452) , MANUFACTURE(72288-452)
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