Bepotastine Besilate Solution
Product Images NDC 70069-712

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Bepotastine Besilate (NDC 70069-712). 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 Bepotastine Besilate, showing the molecular arrangement including the bepotastine portion and the besilate (sulfonate) moiety.*

FDA Label Image

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Label for Bepotastine Besilate Ophthalmic Solution 1.5%, a topical ophthalmic sterile solution. The 5 mL container is manufactured for Somerset Therapeutics, LLC, Somerset, NJ, and made in India. Instructions indicate a usual dosage of one drop in the affected eye twice daily. Label includes storage temperature and barcode details.*

FDA Label Image

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Packaging label for Bepotastine Besilate Ophthalmic Solution 1.5%, a sterile ophthalmic solution for topical use by Somerset Therapeutics LLC. The 5 mL solution contains 15 mg/mL of active ingredient bepotastine besilate. The label includes dosage instructions, inactive ingredients, preservative details, storage conditions, and barcode information.*

FDA Label Image

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Label for Bepotastine Besilate 1.5% Ophthalmic Solution, a sterile eye drop manufactured for Somerset Therapeutics, LLC. The label includes storage instructions (15° to 25°C), usual dosage directions (one drop in affected eye(s) twice daily), and a 10 mL bottle size. It identifies the product as prescription only, made in India, and for topical ophthalmic use.*

FDA Label Image

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Packaging label for Bepotastine Besilate Ophthalmic Solution 1.5%, a 10 mL sterile topical eye drop manufactured for Somerset Therapeutics, LLC. The label includes the NDC 70069-712-01 and details the active ingredient concentration of 15 mg/mL. The label also shows storage information, inactive ingredients, and dosage instructions to instill one drop twice daily in affected eyes.*

* 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.