Betamethasone Dipropionate 0.05% / Niacinamide 4%
Product Images NDC 72934-2026

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 Betamethasone Dipropionate 0.05% / Niacinamide 4% (NDC 72934-2026). 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.

Product Images & Figures Index

FDA Label Image

Fs (2 End)

Fs (2 End)
Label of BETAMETHASONE DIPROPIONATE 0.05% / NIACINAMIDE 4% showing directions for use including application instructions and storage conditions. The label includes the manufacturer Sincerus Florida, LLC with contact information, and a QR code at the bottom left corner. The container is white with black text.*
FDA Label Image

Sf (2026 2 Front)

Sf (2026 2 Front)
Packaging label of BETAMETHASONE DIPROPIONATE 0.05% / NIACINAMIDE 4% cream, 30 gm by Sincerus Florida, LLC. The label includes the NDC number 72934-2026-2 and states the product is a compounded drug made in the USA.*
FDA Label Image

Wr (2026 2 Middle)

Wr (2026 2 Middle)
Label on a pharmaceutical container for BETAMETHASONE DIPROPIONATE 0.05% / NIACINAMIDE 4% cream by Sincerus Florida, LLC. The label includes active ingredients Betamethasone Dipropionate USP 0.05% and Niacinamide USP 4%, and inactive ingredients Kriegel 100 at 1% and a cream base at 94.95%. Additional details include Rx only, expiration date (01/01/1970), lot number 091048ABCDEFG@1, and manufacturing date 01/01/1970.*

* 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.