Azelastine Hydrochloride Spray, Metered
FDA Label NDC 73581-500

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Yyba Corp for the product Azelastine Hydrochloride (NDC 73581-500). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, purpose, uses, warnings, do not use, ask a doctor before use if you, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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 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

  • 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.

Package Label-Principal Display Panel - Container Label (11 Ml Bottle)

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)


Package Label-Principal Display Panel - Container Carton Label (11 Ml Bottle)

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)


* Please review the disclaimer below.