Travoprost Solution/ Drops
Product Images NDC 70069-587

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Travoprost (NDC 70069-587). 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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Chemical structure diagram of the active ingredient Travoprost (Isomer Free), showing its molecular composition and bonds.*

FDA Label Image

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Label for Travoprost Ophthalmic Solution USP 0.004% (0.04 mg/mL) in a 2.5 mL sterile solution. The label indicates the product is for topical ophthalmic use, provides storage instructions (2°C to 25°C), and lists Somerset Therapeutics, LLC as the manufacturer, with production stated as made in India. The label includes an NDC code and a barcode.*

FDA Label Image

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Carton label for Travoprost Ophthalmic Solution, USP 0.004% (0.04 mg/mL) sterile drops in a 2.5 mL bottle. The label includes the active ingredient travoprost, inactive ingredients, usage instructions, storage conditions, and the labeler Somerset Therapeutics LLC. The packaging features the NDC 70069-586-01 and a graphic of an eye.*

FDA Label Image

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Label for Travoprost Ophthalmic Solution, USP 0.004% (0.04 mg/mL) in a 5 mL bottle. The product is sterile and for topical ophthalmic use only. Manufactured for Somerset Therapeutics, LLC, Somerset, NJ, and made in India. The label includes NDC 70069-587-01 and storage instructions between 2°C and 25°C (36°F to 77°F).*

FDA Label Image

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Carton label for Travoprost Ophthalmic Solution, USP 0.004% by Somerset Therapeutics LLC. The label shows the product as a sterile ophthalmic solution in a 5 mL bottle. Active ingredient is travoprost 0.04 mg per mL, with listed inactive ingredients. The label includes storage instructions and patient use directions. National Drug Code 70069-587-01 is displayed.*

* 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.