Dorzolamide Hydrochloride Solution/ Drops
Product Images NDC 61314-019

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dorzolamide Hydrochloride (NDC 61314-019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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

Dorzolamide 01

Chemical structure of dorzolamide hydrochloride, the active ingredient in DORZOLAMIDE HYDROCHLORIDE ophthalmic solution 20 mg/mL by Sandoz Inc.*

FDA Label Image

Dorzolamide 02

Three black-and-white instructional illustrations demonstrate proper handling and administration of an ophthalmic solution bottle. The images show how to hold the bottle with one hand, position the hand over the eye, and dispense drops carefully. These illustrations likely correspond to usage directions for the dorzolamide hydrochloride ophthalmic solution.*

FDA Label Image

Dorzolamide 03

Three-panel illustration showing the steps for using ophthalmic solution drops. The first panel depicts a person pulling down their lower eyelid to create a pocket. The second panel shows the eye with the pocket created for the drop. The third panel illustrates the administration of an eye drop from a dropper bottle held above the eye.*

FDA Label Image

Dorzolamide 04

Packaging label for Dorzolamide HCl Ophthalmic Solution 2% by Sandoz Inc. The sterile ophthalmic solution contains 20 mg/mL dorzolamide equivalent, supplied in a 10 mL bottle. Manufactured by Alcon Laboratories, the label includes storage instructions, inactive ingredients, preservative information, and a barcode.*

* 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.