Product Images Bepotastine Besilate

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Product Label Images

The following 2 images provide visual information about the product associated with Bepotastine Besilate NDC 24208-630 by Bausch & Lomb Incorporated, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Bepreve chemical structure - 995F4FE0 D861 4137 8090 A8FFC71C46F4 00

Bepreve chemical structure - 995F4FE0 D861 4137 8090 A8FFC71C46F4 00

carton - image 01

carton - image 01

Bepotastine Besilate Ophthalmic Solution is a sterile solution used for topical ophthalmic use to treat eye allergies. Each mL contains 15mg of bepotastine besilate, which is equivalent to 10.7mg of bepotastine, along with inactive ingredients such as monobasic sodium phosphate dihydrate, sodium chloride, sodium hydroxide to adjust the pH, and water for injection, USP. The solution also contains a preservative called benzalkonium chloride in the amount of 0.005%. This product is manufactured by Bausch & Lomb, Tampa, Florida, under license from Senju Pharmaceutical Co., Ltd., Osaka, Japan. The product is patented under US Patent Numbers 8,784,789 and 8,877,168. The usual dosage of Bepotastine Besilate Ophthalmic Solution is one drop in the affected eye(s) twice a day. It is advised to instruct patients on precautions to avoid contamination. The product should be stored between 15°C to 25°C (59°F to 77°F). The NDC (National Drug Code) is 24208-630-05. Overall, this is a prescription drug used to treat allergic reactions.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.