Azelastine AH 73581-500

Manufacturer
YYBA Corp
Effective date
2026-07-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-07-25 05:10:21

Label at a glance#

ProductAZELASTINE HYDROCHLORIDE
Active ingredientAZELASTINE HYDROCHLORIDE
Label structure16 sections

Indications and uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: ■ nasal congestion ■ runny nose ■ sneezing ■ itchy nose

Dosage and administration

■ 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...

Storage and handling

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.

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each spray)

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

Purpose

OTC - PURPOSE SECTION

Antihistamine

Uses

INDICATIONS & USAGE SECTION

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

■ nasal congestion ■ runny nose ■ sneezing ■ itchy nose

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you

OTC - ASK DOCTOR SECTION

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

When using this product

OTC - WHEN USING SECTION

■  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

OTC - STOP USE SECTION

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ 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 spraysin 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 spraysin each nostril in a 24 hour period
children under 6 years
do not use

Other information

STORAGE AND HANDLING SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

IMPORTANT INFORMATION FOR USE

SPL UNCLASSIFIED SECTION

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.
1 AZ1 AZ

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.

2 AZ2 AZ


• 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.

3 Az3 Az
TILT HEAD DOWNWARD

STEP 3

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

4 AZ4 AZ


STEP 4

Close one nostril.



5 AZ5 AZ

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).

6 AZ6 AZ

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.

7 AZ7 AZ

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? 866-933-6337

Distributed by:
Wellspring Meds
Airmont, NY 10952

Made in India

Code: AP/DRUGS/04/2016

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WELMATE

NDC 73581-500-01


Azelastine Hydrochloride
Nasal Spray
205.5 mcg per spray

ANTIHISTAMINE NASAL SPRAY

ALLERGY +
CONGESTION

120 METERED SPRAYS
0.78 fl oz (23 mL)


88

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WELMATE

NDC 73581-500-01
*Compare to the active
ingredient in ASTEPRO ®ALLERGY

Azelastine Hydrochloride
Nasal Spray
205.5 mcg per spray
ANTIHISTAMINE NASAL SPRAY
ALLERGY +
CONGESTION

FULL PRESCRIPTION STRENGTH


STEROID FREE
Alcohol-Free
Fragrance-Free

UP TO
24 HOUR
RELIEF OF

• Nasal congestion
• Runny nose
• Sneezing
• Itchy nose

120 METERED SPRAYS
0.78 fl oz (23 mL)


cartoncarton

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73581-50073581-500-01, 73581-500-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-07-14daily-update2026-07-18 05:11:05

Orange Book application contexts#

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Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A216561-001AZELASTINE HYDROCHLORIDE ALLERGYAZELASTINE HYDROCHLORIDE0.2055MG/SPRAYSPRAY, METERED / NASAL2025-01-27

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A216561-001AZELASTINE HYDROCHLORIDE ALLERGY0.2055MG/SPRAYSPRAY, METERED / NASAL2025-01-2784e616aacf4f…
2026-08-18 06:07:402026-07A216561-001AZELASTINE HYDROCHLORIDE ALLERGY0.2055MG/SPRAYSPRAY, METERED / NASAL2025-01-27caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A216561-001AZELASTINE HYDROCHLORIDE ALLERGY0.2055MG/SPRAYSPRAY, METERED / NASAL2025-01-27011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A216561-001AZELASTINE HYDROCHLORIDE ALLERGY0.2055MG/SPRAYSPRAY, METERED / NASAL2025-01-2731067a03dcf5…
2025-08-23 18:47 UTC2025-08A216561-001AZELASTINE HYDROCHLORIDE ALLERGY0.2055MG/SPRAYSPRAY, METERED / NASAL2025-01-276a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A216561-001AZELASTINE HYDROCHLORIDE ALLERGY0.2055MG/SPRAYSPRAY, METERED / NASAL2025-01-27fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A216561-001AZELASTINE HYDROCHLORIDE ALLERGY0.2055MG/SPRAYSPRAY, METERED / NASAL2025-01-27b8a1b40f171c…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A216561-001AZELASTINE HYDROCHLORIDE ALLERGY0.2055MG/SPRAYSPRAY, METERED / NASAL2025-01-27a50c72e98297…

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AZELASTINE HYDROCHLORIDEAZELASTINE HYDROCHLORIDEYYBA Corp52f67910-11a7-6e7d-e063-6394a90ac9e82026-07-22WarningsExact identifier
ndc (package): 73581-500-02
ndc (package): 73581-500-01
ndc (product): 73581-500
ndc11 (package): 73581050002
ndc11 (package): 73581050001
spl id: 57343d7c-0900-e362-e063-6394a90afc09
spl set id: 52f67910-11a7-6e7d-e063-6394a90ac9e8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.