Label: AZELASTINE HYDROCHLORIDE spray, metered

  • NDC Code(s): 58602-020-07, 58602-020-51, 58602-020-52
  • Packager: Aurohealth LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated January 31, 2025

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

  • Drug Facts

    Active ingredient (in each spray)

    Azelastine hydrochloride USP 205.5 mcg (equivalent to 187.6 mcg azelastine)

  • Purpose

    Antihistamine

  • Uses

    temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

    ■ nasal congestion ■ runny nose ■ sneezing ■ itchy nose

  • Warnings

    Only for use in the nose. Do not spray in eyes or mouth.

  • 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 had recent nose ulcers or nose surgery 
     ■  have had a nose injury that has not healed

  • When using this product

    ■  drowsiness may occur 
          ■ avoid alcoholic drinks
          ■ alcohol, sedatives, and tranquilizers may increase drowsiness
          ■ be careful when driving a motor vehicle or operating machinery


    ■ you may get a bitter taste in your mouth. To help avoid this, tilt your head downward while spraying.

    ■ nasal discomfort or sneezing may occur right after use

    ■ do not share this bottle with anyone else as this may spread germs

  • Stop use and ask a doctor if

    ■  an allergic reaction, such as a skin rash, to this product occurs 
    ■  you have severe or frequent nosebleeds

  • 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

    ■ Read the User Guide for how to:

        ■ prime the bottle before first use                              ■ use the spray

        ■ prime bottle again if not used for 3 or more days   ■ clean the spray nozzle if it gets clogged

    adults and children 12 years and older
    This product may be used either once or twice a day:
    once daily: use 2 sprays in each nostril; OR
    twice daily: use 1 or 2 sprays in each nostril every 12 hours
    do not use more than 4 sprays in each nostril in a 24 hour period
    children 6 years to 11 years
    ■ an adult should supervise use
    ■ 1 spray in each nostril every 12 hours
    do not use more than 2 sprays in each nostril in a 24 hour period
    children under 6 years
    do not use
  • Other information

    • store between 20° to 25°C (68° to 77°F). Protect from freezing.
    • keep this carton and the enclosed User Guide for important information
    • do not use if seal printed with “sealed for your protection” on top and bottom carton flaps is not intact.
  • Inactive ingredients

    benzalkonium chloride, edetate disodium, hypromellose, purified water, sodium citrate (dihydrate), sorbitol and sucralose.


    Questions or comments?  1-855-274-4122  (Monday – Friday 8:30 AM to 5:00 PM EST)


    Distributed by:
    AUROHEALTH LLC
    279 Princeton-Hightstown Road
    East Windsor, NJ 08520

    Made in India

    Code: AP/DRUGS/04/2016

  • User Guide

    Azelastine Hydrochloride Nasal Spray 205.5 mcg per spray


    HOW TO START GETTING STEROID-FREE ALLERGY RELIEF RIGHT NOW


    This User Guide will give you detailed directions on how to prime the bottle, use the spray, and how to clean a clogged nozzle.


    Keep this User Guide as it contains important information.


    GET THE BOTTLE READY


    Remove the transparent cap and white clip before using.
    FIgure A


    PRIME THE BOTTLE


    WHEN TO PRIME


    • Before you use Azelastine Hydrochloride Nasal Spray for the first time
    • If you have not used Azelastine Hydrochloride Nasal Spray for 3 or more days
    • After you clean a clogged nozzle

    HOW TO PRIME


    • Aim bottle away from face.

    • Hold bottle as shown and pump until a fine mist appears.

    Figure 2


    • If a fine mist does not appear after 6 sprays, your nozzle may be clogged. Please see “How to Clean a Clogged Nozzle” section.

    HOW TO USE


    Important: For use in your nose only


    STEP 1

    Blow your nose to clear your nostrils.


    STEP 2

    Tilt your head downward toward your toes.

    FIgure C
    TILT HEAD DOWNWARD

    STEP 3

    Hold bottle with thumb under bottle and spray nozzle between fingers.

    FIgure D


    STEP 4


    Close one nostril.



    FIgure E

    HOLD ONE NOSTRIL SHUT

    STEP 5


    Put the spray tip about ¼ inch to ½ inch into the other nostril. Hold bottle upright and aim the spray tip toward the back of your nose.


    STEP 6


    While sniffing gently, press the pump once or twice (according to dosing directions found in Table 1).

    Repeat Steps 4, 5 and 6 in other nostril.


    STEP 7


    Do not tilt your head back immediately after using Azelastine Hydrochloride Nasal Spray. This will help to keep the medicine from going into your throat, which may cause a bitter taste.


    STEP 8


    When you finish using your Azelastine Hydrochloride Nasal Spray, wipe the spray tip with a clean tissue or cloth. Put the clip and cap back on the bottle.


    FOR USE IN CHILDREN

    An adult should supervise use.

    (See Steps 1 through 8).


    SELECT THE DOSE


    DIRECTIONS


    Do not use more than directed


    TABLE 1


    adults & children 12 years and older
    This product may be used either once or twice a day:
    once daily: use 2 sprays in each nostril; OR
    twice daily: use 1 or 2 sprays in each nostril every 12  hours
    do not use more than 4 sprays in each nostril in a 24 hour period
    children 6 years to 11 years
    ■ an adult should supervise use
    ■ 1 spray in each nostril every 12 hours
    do not use more than 2 sprays in each nostril in a 24 hour period
    children under 6 years
    do not use

    IMPORTANT INFORMATION FOR USE


    Remember, when using this product:


    • Drowsiness may occur*

    › Avoid alcoholic drinks.

    › Alcohol, sedatives, and tranquilizers may increase drowsiness.

    › Be careful when driving a motor vehicle or operating machinery.

    *In clinical trials, drowsiness was observed in less than 4% of patients taking Azelastine Hydrochloride Nasal Spray.


    HOW TO CLEAN A CLOGGED NOZZLE


    If you cannot get your Azelastine Hydrochloride Nasal Spray to spray a fine mist, the nozzle may be clogged. Don’t try to unclog the nozzle with a pin or sharp object—that can damage it.

    • Unscrew the spray pump unit from the bottle by turning it to the left (counter-clockwise).

               fig6

    • Keep open bottle out of reach of children.
    • Fill a bowl or container with warm water. Soak only the spray pump unit in the warm water. Pump the nozzle several times while holding it under the water to clear the clog.

            fig7

    • Let the spray pump unit air dry before putting it back on.
    • Tightly screw pump unit back on the open bottle by turning clockwise (to the right).
    • After cleaning, follow the instructions for priming.

    QUESTIONS OR COMMENTS? 1-855-274-4122 (Monday – Friday 8:30 AM to 5:00 PM EST)


    Distributed by:
    AUROHEALTH LLC
    279 Princeton-Hightstown Road
    East Windsor, NJ 08520

    Made in India

    Code: AP/DRUGS/04/2016

    Revised: 01/2024

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - Container Label (11 mL Bottle)

    AUROHEALTH

    NDC 58602-020-51

    Azelastine Hydrochloride
    Nasal Spray
    205.5 mcg per spray

    ANTIHISTAMINE NASAL SPRAY

    Allergy


               60 METERED SPRAYS
               0.37 fl oz (11 mL)



    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - Container Label (30 mL Bottle)

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - Container Carton Label (11 mL Bottle)

    AUROHEALTH

    NDC 58602-020-51
                                 *Compare to the active
                  ingredient in ASTEPRO® ALLERGY

    ANTIHITAMINE
    NASAL SPRAY
     

    Azelastine Hydrochloride 
    Nasal Spray
    205.5 mcg per spray

                 ANTIHISTAMINE NASAL SPRAY
    Allergy 
                FULL PRESCRIPTION STRENGTH


                                STEROID FREE
                                 Alcohol-Free
                                Fragrance-Free

    UP TO
    24 HOUR
    RELIEF OF

    •   Nasal congestion
    •   Runny nose
    •   Sneezing
    •   Itchy nose

                      60 METERED SPRAYS
                      0.37 fl oz (11 mL)

    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - Container Carton Label (30 mL Bottle)


                                

  • INGREDIENTS AND APPEARANCE
    AZELASTINE HYDROCHLORIDE 
    azelastine hydrochloride spray, metered
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58602-020
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AZELASTINE HYDROCHLORIDE (UNII: 0L591QR10I) (AZELASTINE - UNII:ZQI909440X) AZELASTINE HYDROCHLORIDE205.5 ug
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35)  
    WATER (UNII: 059QF0KO0R)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorWHITE (clear colorless) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58602-020-511 in 1 CARTON01/27/2025
    160 in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    2NDC:58602-020-521 in 1 CARTON01/27/2025
    2120 in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    3NDC:58602-020-071 in 1 CARTON01/27/2025
    3200 in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21656101/27/2025
    Labeler - Aurohealth LLC (078728447)
    Establishment
    NameAddressID/FEIBusiness Operations
    APL HEALTHCARE LIMITED650918514ANALYSIS(58602-020) , MANUFACTURE(58602-020)