Bepreve Solution/ Drops
Product Images NDC 24208-629

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bepreve (NDC 24208-629). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bausch & Lomb Incorporated, 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

Carton 10ml

BEPREVE is a sterile ophthalmic solution containing bepotastine besilate used to treat eye allergies. It is distributed by Bausch Health US LLC and manufactured by Bausch & Lomb Incorporated in Tampa, FL under license from Senju Pharmaceutical Co, Ltd in Osaka, Japan. The product comes in a 10 mL container and is available in 1.5% and 15% concentrations. The usual dosage is one drop applied to each affected eye twice a day. The solution contains active and inactive ingredients with benzalkonium chloride as the preservative. It is important to instruct patients on precautions to avoid contamination. Store the unopened container at a temperature between 15 and 25 degrees Celsius.*

FDA Label Image

Carton 5ml

BEPREVE(bepotastine besilate ophthalmic solution) is a sterile 15% 5mL prescription medication used to treat eye allergies. Each mL contains 15 my of bepotastine besilate. To use, one drop should be instilled into the affected eye(s) twice a day. This medication is manufactured by and distributed by Bausch & Lomb, a division of Bausch Health US, LLC. It is sterile when manufactured and should be used only from the original unopened container to avoid contamination. It should be stored at 15°C to 25°C. No non-English characters found.*

FDA Label Image

Chemical Structure (E8c7bd70 E024 4a70 81c9 0bf4a35e3b3c 01)

* 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.