Cosopt Solution/ Drops
Product Images NDC 82584-605

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Cosopt (NDC 82584-605). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Thea Pharma Inc., 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

Chemical Structure (Cosopt 01)

Chemical Structure (Cosopt 01)
Chemical structure diagram of dorzolamide hydrochloride, the active ingredient in COSOPT ophthalmic solution. The structure includes a sulfonamide group, a thiophene ring, and a hydrochloride component.*
FDA Label Image

Chemical Structure (Cosopt 02)

Chemical Structure (Cosopt 02)
Chemical structure diagram showing the active ingredients dorzolamide hydrochloride and timolol maleate, as indicated by their molecular components in the structure.*
FDA Label Image

Figure A (Cosopt 03)

Figure A (Cosopt 03)
An instructional illustration showing the proper technique for administering ophthalmic solution drops. A hand is depicted holding an eye drop bottle above a downward-facing eye, demonstrating how to apply drops into the eye.*
FDA Label Image

Figure B (Cosopt 04)

Figure B (Cosopt 04)
An instructional illustration showing a person administering ophthalmic solution eye drops. The image depicts one hand holding the eye open while the other hand squeezes a dropper bottle to release a drop into the eye.*
FDA Label Image

Principal Display Panel (10 mL Bottle Carton)

Principal Display Panel (10 mL Bottle Carton)
COSOPT ophthalmic solution 2%/0.5% (dorzolamide hydrochloride 22.3 mg/mL and timolol maleate 6.8 mg/mL) sterile eye drops in a 10 mL bottle. The label displays Thea Pharma Inc. as the manufacturer and includes storage instructions, inactive ingredients, and the NDC number 82584-605-10. The packaging is primarily dark blue and white with barcodes and usage warnings for topical ophthalmic application.*

* 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.