Dorzolamide Hydrochloride And Timolol Maleate Preservative Free Solution/ Drops
Product Images NDC 65862-947

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Dorzolamide Hydrochloride And Timolol Maleate Preservative Free (NDC 65862-947). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Figure A (Dorzolamide Timolol Fig1)

An instructional illustration depicting a hand holding a small ophthalmic dropper bottle upright, labeled as Figure A. The image appears to demonstrate the proper way to hold the eye drop bottle before administration.*

FDA Label Image

Figure B (Dorzolamide Timolol Fig2)

An instructional diagram labeled Figure B shows hands manipulating a small ophthalmic dropper bottle by pinching the body and securing the cap or dropper tip, demonstrating proper handling of the solution drops.*

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Figure C (Dorzolamide Timolol Fig3)

Illustration showing a person tilting their head back and instilling eye drops into the lower eyelid using a dropper, demonstrating proper technique for ophthalmic solution administration.*

FDA Label Image

Figure D (Dorzolamide Timolol Fig4)

An instructional illustration showing a person administering ophthalmic solution drops into the eye. The hand holds a dropper bottle above the eye, with the other hand gently pulling down the lower eyelid to create a pocket for the drops.*

FDA Label Image

Package Label-principal Display Panel (2%/0.5% (BFS LDPE Vial Label))

Label of Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution, USP, showing strengths 2% and 0.5% (base). The solution is preservative free, for ophthalmic use, prescription only, manufactured in India for Aurobindo Pharma Limited.*

FDA Label Image

Package Label-principal Display Panel (2%/0.5% (Pouch Label)

Label for Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution, USP, 2% / 0.5%, preservative free, for topical eye application. The package contains 15 single-use containers with 0.2 mL each. Distributed by Aurobindo Pharma USA, Inc., made in India. The label includes active and inactive ingredients, storage instructions, dosage directions, and a barcode.*

FDA Label Image

Package Label-principal Display Panel (2%/0.5% (Container-Carton)

Packaging label for Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution, USP 2% / 0.5%, preservative free, for topical application in the eye. The label indicates a pack of 60 single-use containers (4 pouches x 15 containers) each with 0.2 mL solution. Distributed by Aurobindo Pharma USA, Inc., made in India. Includes storage, usage, and ingredient information.*

FDA Label Image

Package Label-principal Display Panel (2%/0.5% (Carton Label)

Label of Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution, USP 2% / 0.5% preservative free, for topical application in the eye. The product contains 180 single-use containers of 0.2 mL each, packaged in 12 pouches of 15 containers. Distributed by Aurobindo Pharma USA, Inc. The label includes storage and usage instructions.*

FDA Label Image

Chemical Structure (Dorzolamide Timolol Str1)

Chemical structure diagram of Dorzolamide Hydrochloride and Timolol Maleate Preservative Free, displaying the molecular components and bonds characteristic of the active ingredients in this ophthalmic solution.*

FDA Label Image

Chemical Structure (Dorzolamide Timolol Str2)

Chemical structure diagram of the active ingredient in Dorzolamide Hydrochloride and Timolol Maleate Preservative Free ophthalmic solution. The structure depicts molecular components typical for dorzolamide, showing atoms and bonds in a detailed chemical formula.*

* 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.