Dorzolamide Hydrochloride And Timolol Maleate Solution/ Drops
Product Images NDC 50742-323

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Dorzolamide Hydrochloride And Timolol Maleate (NDC 50742-323). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ingenus Pharmaceuticals, 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 of dorzolamide hydrochloride, showing the molecular arrangement including sulfonamide and thiophene groups, paired with hydrochloride as indicated.*
FDA Label Image

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Chemical structure of dorzolamide hydrochloride and timolol maleate, showing molecular connectivity including a morpholine ring, thiadiazole moiety, and carboxyl groups.*
FDA Label Image

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FDA Label Image

Dorzolamide Hydrochloride And Timolol Maleate Ophthalmic Solution (Container Label)

Dorzolamide Hydrochloride And Timolol Maleate Ophthalmic Solution (Container Label)
A product label for Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution, USP. The label indicates strengths of 2% and 0.5%, respectively, and notes that the solution is preservative free. Fields for lot number and expiration date are present but not filled in. The label features the number 3090 prominently on the left side.*
FDA Label Image

Dorzolamide Hydrochloride And Timolol Maleate Ophthalmic Solution (Pouch Label)

Dorzolamide Hydrochloride And Timolol Maleate Ophthalmic Solution (Pouch Label)
Label for Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution, USP 2% / 0.5%, a sterile preservative-free eye drop solution. The label states active ingredient strengths per mL and includes storage instructions, usage warnings, and dosage information. Packaging contains 5 single-use containers each with 0.2 mL, manufactured by Ingenus Pharmaceuticals, LLC.*
FDA Label Image

Dorzolamide Hydrochloride And Timolol Maleate Ophthalmic Solution (Carton Label)

Dorzolamide Hydrochloride And Timolol Maleate Ophthalmic Solution (Carton Label)
Packaging label for Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution, USP 2% / 0.5%, a sterile, preservative-free ophthalmic solution. Each box contains 60 single-use containers (12 pouches of 5 containers, 0.2 mL each). Labeler is Ingenus Pharmaceuticals, LLC. The label includes storage instructions, active and inactive ingredients, dosing directions, and barcodes with NDC 50742-323-60.*
FDA Label Image

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FDA Label Image

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An instructional illustration labeled Figure A showing a hand holding a small ophthalmic dropper bottle upright, demonstrating the proper way to hold the bottle for eye drop administration.*
FDA Label Image

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An instructional illustration showing two hands opening a single-dose container by twisting or pulling apart its top portion. The image is labeled as Figure B, commonly used for ophthalmic solution single-use vials.*
FDA Label Image

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An instructional illustration showing a person administering ophthalmic drops. The person is tilting their head back slightly while using one hand to hold the eye open and the other to squeeze drops from a dropper above the eye. The figure is labeled as Figure C.*
FDA Label Image

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An instructional illustration showing a person administering ophthalmic drops. The person is tilting their head back, using one hand to pull down the lower eyelid, and holding a dropper above the eye with the other hand to apply the solution.*
FDA Label Image

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* 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.