Calcipotriene 0.005% / Triamcinolone Acetonide 0.1%
Product Images NDC 72934-5034

3 FDA label images from Sincerus Florida, Llc · 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 0.005% / Triamcinolone Acetonide 0.1% (NDC 72934-5034). 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

A (5034 3 End)

A (5034 3 End)
CALCIPOTRIENE 0.005% / TRIAMCINOLONE ACETONIDE 0.1% topical medication in a white cylindrical container. The label shows directions for use, storage instructions, and contact information for the labeler, Sincerus Florida, LLC, based in Pompano Beach, FL. The product is intended for topical application under physician direction.*
FDA Label Image

C (5034 3 Front)

C (5034 3 Front)
CALCIPOTRIENE 0.005% / TRIAMCINOLONE ACETONIDE 0.1% ointment in a 60 gm white cylindrical container. The label includes the NDC 72934-5034-3 and the Sincerus Florida logo. The product is identified as a compounded drug made in the USA by Sincerus Florida, LLC.*
FDA Label Image

E (5034 3 Middle)

E (5034 3 Middle)
CALCIPOTRIENE 0.005% / TRIAMCINOLONE ACETONIDE 0.1% ointment in a white cylindrical container with a label showing active ingredients (Calcipotriene Anhydrous USP 0.005%, Triamcinolone Acetonide USP 0.1%) and inactive ingredient (Petrolatum 99.895%). The label indicates the product is Rx only and is manufactured by Sincerus Florida, LLC.*

* 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.