Calcipotriene Ointment
Product Images NDC 66993-878

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Calcipotriene (NDC 66993-878). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Prasco Laboratories, 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

Calcipotriene Structure (Calc Structure)

Calcipotriene Structure (Calc Structure)
Chemical structure of calcipotriene, depicted as a molecular diagram with labeled atoms and bonds.*
FDA Label Image

Principal Display Panel (60 g Tube Carton)

Principal Display Panel (60 g Tube Carton)
Packaging label for Calcipotriene Ointment, 0.005% strength, topical ointment by Prasco Laboratories. The label includes the active ingredient concentration as 0.05 mg per gram, net weight of 60 g, barcode, storage instructions, manufacturer details, and usage warnings. It also displays the Rx only designation and the NDC code 66993-878-61.*
FDA Label Image

Principal Display Panel (120 g Tube Carton)

Principal Display Panel (120 g Tube Carton)
The packaging label for Calcipotriene Ointment, 0.005% strength, topical ointment by Prasco Laboratories. The label includes a warning to keep out of reach of children and usage instructions for topical dermatologic use only. The net weight is 120 grams, and the product is Rx only. Storage instructions specify controlled room temperature of 15-25°C (59-77°F) and not to freeze. The manufacturing details show it is made by LEO Laboratories Ltd., Ireland, and manufactured for Prasco Laboratories, Mason, OH.*

* 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.