Azelastine Hydrochloride Spray, Metered
Product Images NDC 58602-020

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Azelastine Hydrochloride (NDC 58602-020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Figure A (Azelastine Fig1)

Figure A (Azelastine Fig1)
An instructional illustration demonstrating the removal of the cap from a nasal spray bottle, showing a hand holding the bottle and another hand pulling the cap upward and away.*
FDA Label Image

Figure 2 (Azelastine Fig2)

Figure 2 (Azelastine Fig2)
An instructional illustration showing a hand pressing down on a nasal spray bottle nozzle to administer a spray. The diagram highlights the spray being released from the bottle nozzle, indicating correct use of the metered nasal spray.*
FDA Label Image

Figure C (Azelastine Fig3)

Figure C (Azelastine Fig3)
An instructional illustration showing the proper use of a metered nasal spray. The image depicts a hand holding a nasal spray bottle being positioned at the nostril of a person's face for administration.*
FDA Label Image

Figure D (Azelastine Fig4)

Figure D (Azelastine Fig4)
An instructional line drawing showing how to hold and use a nasal spray bottle. The illustration depicts one hand supporting the bottom of the bottle while the other hand presses down on the pump actuator at the top to deliver the spray.*
FDA Label Image

Figure E (Azelastine Fig5)

Figure E (Azelastine Fig5)
An instructional line drawing depicting a person using a nasal spray. The individual holds the spray bottle with one hand and uses a finger from the other hand to gently close one nostril, demonstrating the proper technique for administering a nasal spray into the open nostril.*
FDA Label Image

Fig6 (Azelastine Fig6)

Fig6 (Azelastine Fig6)
An instructional diagram showing two hands unscrewing the pump unit from a container. The image focuses on the manual action needed to separate the parts, with the accompanying text "UNSCREW PUMP UNIT" below the illustration, indicating a step in the use or assembly process of the nasal spray product.*
FDA Label Image

Fig7 (Azelastine Fig7)

Fig7 (Azelastine Fig7)
An instructional illustration showing a hand holding a nasal spray pump nozzle underwater, with droplets indicating spray. Text below instructs: "Pump nozzle while holding it underwater." This visual guides proper cleaning or use of the spray nozzle.*
FDA Label Image

Package Label-principal Display Panel (Container Label (30 mL Bottle))

Package Label-principal Display Panel (Container Label (30 mL Bottle))
Label for Azelastine Hydrochloride Nasal Spray 205.5 mcg per spray by Aurohealth LLC. It is an antihistamine nasal spray with 60 metered sprays in a 0.37 fl oz (11 mL) bottle. The label includes usage warnings, storage instructions, and distributor information.*
FDA Label Image

Package Label-principal Display Panel (Container Carton Label (30 mL Bottle))

Package Label-principal Display Panel (Container Carton Label (30 mL Bottle))
Packaging label for Azelastine Hydrochloride Nasal Spray 205.5 mcg per spray by Aurohealth LLC. The label indicates a metered nasal spray with 60 sprays (0.37 fl oz, 11 mL). It highlights full prescription strength ant-ihistamine nasal spray for allergy relief, listing symptoms like nasal congestion, runny nose, sneezing, and itchy nose. The label includes drug facts, warnings, directions, and storage instructions.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.