Dorzolamide Hydrochloride
Product Images NDC 50090-1246

5 FDA label images from A-s Medication Solutions · 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 Dorzolamide Hydrochloride (NDC 50090-1246). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Image_1 (Image 01)

FDA Label Image

Image_2 (Image 02)

Image_2 (Image 02)
Chemical structure of Dorzolamide Hydrochloride showing the molecular arrangement, including sulfur, oxygen, nitrogen, hydrogen atoms, and the hydrochloride component.*
FDA Label Image

Image_32 (Image 03)

Image_32 (Image 03)
An instructional line drawing showing a person using their finger to pull down the lower eyelid while preparing to apply eye drops to the eye.*
FDA Label Image

Image 4 (Image 04)

Image 4 (Image 04)
An instructional line drawing illustrating the use of eye drops. The image shows a hand holding a dropper bottle angled above an open eye, with a magnified circular inset detailing a drop falling into the eye. This diagram is likely related to applying Dorzolamide Hydrochloride eye drops.*
FDA Label Image

Label Image (Lbl500901246)

Label Image (Lbl500901246)
Label for Dorzolamide Hydrochloride ophthalmic solution 23.3 mg per mL, equivalent to 20 mg Dorzolamide, provided by A-S Medication Solutions. The 10 mL bottle label includes storage instructions to store between 68 to 77 degrees Fahrenheit and protect from light. The label also shows the product number 6267-0 and NDC 50090-1246-0.*

* 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.