Taclonex Suspension
Product Images NDC 50222-501

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Taclonex (NDC 50222-501). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leo 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.

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This is a description of the medication Taclonex® ERIEERS, which is a topical suspension containing 0.005% calcipotriene and 0.064% betamethasone dipropionate. The medication should only be used topically and should be shaken before use. It comes in a 60-gram container and should be stored between 20°C - 26°C. It should not be refrigerated, and the bottle should be kept in the carton when not in use. The medication should be discarded six months after opening the bottle. It is manufactured by LEO Laboratories Ltd., based in Ireland, and distributed by LEO Pharm Inc. in the US.*

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Taclonex® is a topical suspension medication containing calcipotriene, betamethasone dipropionate, and other ingredients, manufactured by LEO Laboratories Ltd. It is used only for topical use and should be shaken before use. It comes in two bottles of 60 grams each and should be discarded after six months of opening. Each gram contains 50 mg of calcipotriene and 0.643 mg of betamethasone dipropionate on a base of hydrogenated castor oil, butylhydroxytoluene, and mineral oil. It is not recommended to be refrigerated and should be kept between 20°C-25°C (68°F-77°F) and should be kept out of the reach of children. It is distributed by LEO Pharma Inc. in Madison, NJ 07940, USA. Dosage should be taken as per the prescription provided.*

* 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.