Levocetirizine Dihydrochloride 2% / Mupirocin 2% / Triamcinolone Acetonide 0.025%
Product Images NDC 72934-2137

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 Levocetirizine Dihydrochloride 2% / Mupirocin 2% / Triamcinolone Acetonide 0.025% (NDC 72934-2137). 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

X (2 End)

X (2 End)
Label on a white container for LEVOCETIRIZINE DIHYDROCHLORIDE 2% / MUPIROCIN 2% / TRIAMCINOLONE ACETONIDE 0.025%, by Sincerus Florida, LLC. The label includes directions for use, storage information, contact details for reporting adverse reactions, and a QR code. It instructs topical application and controlled room temperature storage (20-25°C).*
FDA Label Image

A (2137 2 Front)

A (2137 2 Front)
A white cylindrical container with a label for LEVOCETIRIZINE DIHYDROCHLORIDE 2%, MUPIROCIN 2%, TRIAMCINOLONE ACETONIDE 0.025% cream, 30gm. Label includes NDC 72934-2137-2 and indicates it is a compounded drug made in the USA by Sincerus Florida, LLC.*
FDA Label Image

X (2137 2 Middle)

X (2137 2 Middle)
A white cylindrical container label for Levocetirizine Dihydrochloride 2%, Mupirocin 2%, Triamcinolone Acetonide 0.025% cream. The label lists active ingredients with their USP percentages and inactive ingredient Versapro Cream. It includes manufacturing and expiry dates, and the lot number. The labeler is 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.