Azelastine Hydrochloride Solution/ Drops
Product Images NDC 70069-091

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Azelastine Hydrochloride (NDC 70069-091). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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

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Chemical structure diagram of Azelastine Hydrochloride, showing its molecular arrangement with rings, nitrogen, oxygen, chlorine atoms, and the hydrochloride component indicated.*

FDA Label Image

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Label for Azelastine Hydrochloride Ophthalmic Solution, USP 0.05%, sterile eye drops. The bottle contains 6 mL of solution, manufactured for Somerset Therapeutics, LLC, Hollywood, FL. Storage instructions specify keeping the product upright between 2°C and 25°C (36°F and 77°F). The label includes an NDC code 70069-091-01 and a barcode.*

FDA Label Image

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Cardboard carton packaging for Azelastine HCl Ophthalmic Solution, USP, 0.05% (0.5 mg/mL) by Somerset Therapeutics LLC. It contains 6 mL sterile eye solution in a 10 mL bottle for ophthalmic use. The label shows dosage instructions, preservative and inactive ingredients, storage conditions, and manufacturer details including a contact number. The package includes multiple barcodes and is marked Rx only.*

* 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.