Calcipotriene 0.005% / Diclofenac Sodium 3% / Hyaluronic Acid Sodium Salt 2% / Niacinamide 2%
Product Images NDC 72934-2030

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Calcipotriene 0.005% / Diclofenac Sodium 3% / Hyaluronic Acid Sodium Salt 2% / Niacinamide 2% (NDC 72934-2030). 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

C (2 End)

Side view of a white cylindrical container for CALCIPOTRIENE 0.005% / DICLOFENAC SODIUM 3% / HYALURONIC ACID SODIUM SALT 2% / NIACINAMIDE 2% by Sincerus Florida, LLC. The visible label includes directions for use and contact information for the labeler, including a phone number and a web address for FDA MedWatch reporting. The label emphasizes external topical use, hand washing after use, and storage at controlled room temperature (20-25°C).*

FDA Label Image

Ds (2030 2 Front)

The image shows a white plastic container labeled with CALCIPOTRIENE ANHYDROUS USP 0.005%, DICLOFENAC SODIUM USP 3%, HYALURONIC ACID SODIUM SALT 2%, and NIACINAMIDE USP 2%. It is a cream formulation with a net weight of 30 grams. The label features the Sincerus Florida logo and notes that this is a compounded drug made in the USA. The NDC listed is 72934-2030-2.*

FDA Label Image

Axs (2030 2 Middle)

Label on a white container lists the active and inactive ingredients of Calcipotriene 0.005% / Diclofenac Sodium 3% / Hyaluronic Acid Sodium Salt 2% / Niacinamide 2% cream. Active ingredients include Calcipotriene Anhydrous USP 0.005%, Diclofenac Sodium USP 3%, Hyaluronic Acid Sodium Salt 2%, and Niacinamide USP 2%. Inactive ingredients include Ethoxy Diglycol Reagent 10%, Methylparaben NF 0.05%, Propylparaben NF 0.025%, and Purified Water USP 82.92%. The label also states Rx only, with a lot number and manufacturing date.*

* 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.