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.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.