Bimatoprost Solution/ Drops
Product Images NDC 70069-401

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Bimatoprost (NDC 70069-401). 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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FDA Label Image

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Bimatoprost is an ophthalmic solution with an active ingredient of 0.3 mg/mL that is used in the eyes only once a day in the evening. It contains benzalkonium chloride as a preservative of 0.05 mg/mL. It is advised to store it at a temperature between 2°-25°C (36°-77°F) and it is manufactured for Somerset Therapeutics, LLC. The product is made in India and has the NDC code 70069-401-01. The code no. KRIDRUGS/KTK/28/289/97 is included as well. This is a prescription drug and comes in a bottle size of 2.5 mL.*

FDA Label Image

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Somerset Therapeutics LLC manufactures Bimatoprost ophthalmic solution for use in the eyes only. It comes in a 2.5mL bottle and contains Bimatoprost 0.3 mg/mL as an active ingredient and benzalkonium chloride 0.05 mg/mL as a preservative. Its pH ranges from 6.8 - 7.8 during its shelf life. The usual dosage is one drop in the affected eye(s) once daily in the evening, and it should be stored at 2° - 25°C (36° - 77°F). The product is filled to 1/2 capacity and is sold under the code number KR/DRUGS/KTK/281289/97, NDC 70069-401-01.*

FDA Label Image

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This is a medication called Bimatoprost used in the eyes only, in a concentration of 0.3mg/mL, with a preservative called Benzalkonium chloride at 0.05mg/mL. The typical dose is one drop in the affected eye(s) once daily in the evening. It should be stored at 2°-25°C. It is manufactured for Somerset Therapeutics, LLC, located in Hollywood, FL, and made in India. The product comes in a 5mL container with the NDC number 70069-402-01 and is only available with a prescription.*

FDA Label Image

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This is a description of an ophthalmic solution called Bimatoprost, manufactured for Somerset Therapeutics LLC in Hollywood, Florida. It is made in India and contains active ingredient Bimatoprost 0.3 mg/mL. It also contains Benzalkonium chloride as a preservative and a combination of citric acid, water, sodium chloride, and sodium phosphate dibasic as inactives. The solution is sterile and should only be used in the eyes. The usual dosage is one drop in the affected eye(s) once daily in the evening. It comes in a 5mL bottle and should be stored between 2° - 25°C (36° - 77°F).*

FDA Label Image

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This is an ophthalmic solution containing Bimatoprost 0.3 mg/mL, with Benzalkonium chloride as preservative. It is used for the treatment of eye conditions, with the recommended dosage of one drop in the affected eye(s) once daily in the evening. The product should be stored at 2°-25°C (36°-77°F). It was manufactured for Somerset Therapeutics, LLC and made in India.*

FDA Label Image

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This is a description of a prescription medication called Bimatoprost Ophthalmic Solution 0.03%, manufactured in India for Somerset Therapeutics LLC based in Hollywood, FL. The product is intended for use in the eyes to treat certain eye conditions. The product contains active ingredient Bimatoprost 0.3 mg/mL and preservative Benzalkonium chloride 0.05 mg/mL. The product is a sterile solution provided in a bottle that is filled to 3/4 capacity. The recommended dosage is one drop in the affected eye(s) once daily in the evening, and the product should be stored at 2° - 25°C (36° - 77°F). The product's NDC number is 70069-403-01.*

* 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.