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

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% / 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)

Sd (4029 5 End)
A drug directions panel on a white bottle for CALCIPOTRIENE 0.005% / CLOBETASOL PROPIONATE 0.05% by Sincerus Florida, LLC. Directions include use as directed by a physician, topical application, washing hands after use, and storage at controlled room temperature. Contact information for reporting adverse reactions is provided, along with a QR code.*
FDA Label Image

Sd (4029 5 Front)

Sd (4029 5 Front)
CALCIPOTRIENE 0.005% / CLOBETASOL PROPIONATE 0.05% solution in a white plastic bottle with a screw cap. The label shows the NDC 72934-4029-5 and identifies the contents as 60 grams of compounded drug. The labeler is Sincerus Florida, LLC, with their logo displayed, and the product is made in the USA.*
FDA Label Image

Cs (4029 5 Middle)

Cs (4029 5 Middle)
A white plastic bottle with a label listing active and inactive ingredients for CALCIPOTRIENE 0.005% / CLOBETASOL PROPIONATE 0.05% solution. The label displays the active ingredients Calcipotriene Anhydrous USP (0.005%) and Clobetasol Propionate USP (0.05%), along with inactive ingredients Ethyl Alcohol USP and Purified Water USP. The label includes manufacturing and expiration information and the lot number.*

* 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.