Dorzolamide Hydrochloride And Timolol Maleate Ophthalmic Solution Solution/ Drops
Product Images NDC 72162-2381

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dorzolamide Hydrochloride And Timolol Maleate Ophthalmic Solution (NDC 72162-2381). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Dorzolamide Structure (Dorzotimo Dorzolamidestrc)

Chemical structure of Dorzolamide Hydrochloride, showing molecular rings, functional groups, and attached atoms, as part of the Dorzolamide Hydrochloride and Timolol Maleate ophthalmic solution product.*

FDA Label Image

Figure B (Dorzotimo Figreb)

Illustration showing the proper administration of Dorzolamide Hydrochloride and Timolol Maleate ophthalmic solution. It depicts a person holding the dropper bottle above an eye, with a drop about to be instilled, indicating the correct method of eye drop application.*

FDA Label Image

Fig A (Dorzotimo Figurea)

An instructional illustration labeled 'Figure A' depicting a hand holding an eye drop bottle and administering a drop into the eye by directing it downward toward the lower eyelid.*

FDA Label Image

Timolol Structure (Dorzotimo Timololstrct)

Chemical structure of Dorzolamide Hydrochloride and Timolol Maleate, the active ingredients in Dorzolamide Hydrochloride and Timolol Maleate ophthalmic solution. The diagram shows the molecular formulae and connectivity of these compounds used in this prescription ophthalmic solution by Bryant Ranch Prepack.*

FDA Label Image

Label (Lbl721622381)

Label for Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution, USP, strength 2%/0.5%, in a 10 mL bottle. The label includes NDC 72162-2381-2, manufacturer Micro Labs Limited, and relabeler Bryant Ranch Prepack, Inc. It provides active ingredient content per mL and storage instructions, with emphasis on ophthalmic use and tamper-evident packaging.*

* 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.