Calcipotriene 0.005% / Clobetasol Propionate 0.05%
Product Images NDC 72934-4029

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Calcipotriene 0.005% / Clobetasol Propionate 0.05% (NDC 72934-4029). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, Llc, 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

Sd (4029 5 End)

This text provides instructions and warnings for the topical use of a product. It advises to only use externally, wash hands after use, and to store at a controlled room temperature. It also gives contact information for adverse reaction reporting to the manufacturer and FDA. It is not available whether there is a description of the product being used.*

FDA Label Image

Sd (4029 5 Front)

This is a description of a medication with the NDC code 72934-4029-5. The medication is a solution containing 0.005% USP calcipotriene anhydrous and 0.05% USP clobetasol propionate. The total package size is 60g. The remaining characters are not readable.*

FDA Label Image

Cs (4029 5 Middle)

The product contains active ingredients including Calcipotriene Anhydrous USP, Clobetasol Propionate USP, Ethyl Alcohol USP, and Purified Water, USP.*

* 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.