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Chemical structure of latanoprost showing its molecular framework with a molecular weight of 432.58.*
Latanoprost Solution/ Drops
Product Images NDC 70069-421
4 FDA label images from Somerset Therapeutics, Llc · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Latanoprost (NDC 70069-421). 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.
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Latanoprost Ophthalmic Solution 0.005% in a 2.5 mL bottle. The label includes dosage strength of 125 mcg/2.5 mL, indicates it is for ophthalmic use and for use in the eyes only. Manufactured by Somerset Therapeutics, LLC, Hollywood, FL, and made in India. Label shows NDC 70069-421-01 with usual dosage instructions of one drop in the affected eye(s) in the evening. The label includes a barcode and packaging dimensions 15 x 10 mm.*
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Packaging label for Latanoprost Ophthalmic Solution 0.005%, 125 mcg/2.5 mL (50 mcg/mL) sterile solution in a 2.5 mL bottle by Somerset Therapeutics, LLC. The label includes NDC 70069-421-01, directions for use in the eyes only, and storage instructions. The design features the product name prominently, dosage strength, and manufacturer details alongside barcodes.*
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Packaging label for Latanoprost Ophthalmic Solution 0.005%, 125 mcg/2.5 mL, in a three 2.5 mL bottle multi-pack. The label shows this is a sterile solution for ophthalmic use only, manufactured by Somerset Therapeutics, LLC. The label includes storage instructions, a barcode, and states it is not to be sold separately.*
* 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.
