Clobetasol Propionate 0.05% / Levocetirizine Dihydrochloride 2%
Product Images NDC 72934-7058

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% / Levocetirizine Dihydrochloride 2% (NDC 72934-7058). 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

Sad (7058 6 End)

Sad (7058 6 End)
A white cylindrical bottle with a flip-top cap labeled with usage directions and manufacturer information. The label includes instructions for topical use, storage conditions, contact information for Sincerus Florida, LLC in Pompano Beach, FL, and a QR code. The product name and dosage are not visible on this side.*
FDA Label Image

Cc (7058 6 Front)

Cc (7058 6 Front)
Bottle of CLOBETASOL PROPIONATE 0.05% / LEVOCETIRIZINE DIHYDROCHLORIDE 2% shampoo, 120 gm, labeled with NDC 72934-7058-6. The label shows the brand name SINERUS FLORIDA and states it is a compounded drug made in the USA.*
FDA Label Image

Fg (7058 6 Middle)

Fg (7058 6 Middle)
A white plastic bottle labeled with active and inactive ingredients for CLOBETASOL PROPIONATE 0.05% / LEVOCETIRIZINE DIHYDROCHLORIDE 2% shampoo. The label lists Clobetasol Propionate USP 0.05% and Levocetirizine Dihydrochloride USP 2% as active ingredients, with Tea Tree Oil, Suspendsse Shampoo, and Zinc Pyrithione 50% Dispersion as inactive ingredients. The label also includes RX only, lot number, manufacturing, and expiration dates. The bottle is marked with the labeler name 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.