Clobetasol Propionate 0.05% / Niacinamide 4%
Product Images NDC 72934-2059

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 Clobetasol Propionate 0.05% / Niacinamide 4% (NDC 72934-2059). 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

R (2059 3 End)

R (2059 3 End)
Container label for CLOBETASOL PROPIONATE 0.05% / NIACINAMIDE 4% by Sincerus Florida, LLC. The label includes directions for use stating it is for external use only, application by a physician, and advises washing hands after use. The label also provides storage instructions and contact information for reporting adverse reactions, including a phone number and FDA website. The container is white with a printed label featuring black text.*
FDA Label Image

S (2059 3 Front)

S (2059 3 Front)
Container of Clobetasol Propionate USP 0.05% and Niacinamide USP 4% cream, 60 grams, labeled as a compounded drug. The label shows the product NDC 72934-2059-3 and the Sincerus Florida logo, indicating the manufacturer. The container is white with a white cap.*
FDA Label Image

R (2059 3 Middle)

R (2059 3 Middle)
CLOBETASOL PROPIONATE 0.05% / NIACINAMIDE 4% cream in a white cylindrical container. The label lists active ingredients as Clobetasol Propionate USP 0.05% and Niacinamide USP 4%, with inactive ingredients comprising 95.95% of the suspension cream. Manufactured by Sincerus Florida, LLC, this is a prescription-only product.*

* 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.