Bimatoprost Solution/ Drops
Product Images NDC 70069-403

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Bimatoprost (NDC 70069-403). 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

Molecuar Structure (93e51046 A2f5 47ab 8aa7 B0d8c9c119eb 01)

Chemical structure diagram of Bimatoprost, showing its molecular framework including hydroxyl groups, a phenyl ring, and an ethylamide side chain.*

FDA Label Image

2.5 mL Container Label (93e51046 A2f5 47ab 8aa7 B0d8c9c119eb 02)

Label for Bimatoprost Ophthalmic Solution 0.03%, an eye drop solution containing 0.3 mg/mL Bimatoprost with preservative benzalkonium chloride 0.05 mg/mL. The label indicates a 2.5 mL bottle, prescription only, manufactured for Somerset Therapeutics, LLC. Storage instructions and barcode are also present.*

FDA Label Image

2.5 mL Carton Label (93e51046 A2f5 47ab 8aa7 B0d8c9c119eb 03)

Label for Bimatoprost Ophthalmic Solution 0.03% in a 2.5 mL sterile solution dosage form. The label includes the active ingredient concentration, preservative benzalkonium chloride 0.05 mg/mL, inactive ingredients, usual dosage, and storage instructions. Manufactured for Somerset Therapeutics LLC, the label highlights the product is for ophthalmic use only and prescription-only with NDC 70069-401-01.*

FDA Label Image

5 mL Container Label (93e51046 A2f5 47ab 8aa7 B0d8c9c119eb 04)

Label for Bimatoprost Ophthalmic Solution 0.03%, a prescription eye drop solution. The label indicates a concentration of 0.3 mg/mL in a 5 mL bottle, manufactured for Somerset Therapeutics, LLC. It includes active ingredient and preservative information, storage instructions, and a barcode.*

FDA Label Image

5 mL Monocarton Label (93e51046 A2f5 47ab 8aa7 B0d8c9c119eb 05)

Label for Bimatoprost Ophthalmic Solution 0.03%, a sterile eye drop solution in a 5 mL container. The label states Rx only, includes the NDC number 70069-402-01, and lists Somerset Therapeutics LLC as the manufacturer. The label notes the active ingredient concentration as 0.3 mg/mL and includes preservative and inactive ingredients. Directions and storage temperature are also partially visible.*

FDA Label Image

7.5 mL Container Label (93e51046 A2f5 47ab 8aa7 B0d8c9c119eb 06)

Label for Bimatoprost Ophthalmic Solution 0.03% . The label indicates it is a prescription eye drop solution containing 0.3 mg/mL Bimatoprost with benzalkonium chloride as a preservative. The packaging shows a 7.5 mL bottle size, manufactured for Somerset Therapeutics, LLC, Somerset, NJ. The label includes usage instructions and storage conditions, with a barcode and lot/expiration printing area.*

FDA Label Image

7.5 mL Monocarton Label (93e51046 A2f5 47ab 8aa7 B0d8c9c119eb 07)

Label for Bimatoprost Ophthalmic Solution 0.03%, an eye drop solution in a 7.5 mL sterile bottle. The label states it is Rx only with NDC 70069-403-01 and manufactured for Somerset Therapeutics LLC. It includes active ingredient concentration (Bimatoprost 0.3 mg/mL), preservative (Benzalkonium chloride 0.05 mg/mL), inactives, storage instructions, and usual dosage directions.*

* 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.