Hydrocortisone 2.5% / Levocetirizine Dihydrochloride 2%
Product Images NDC 72934-2113

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 Hydrocortisone 2.5% / Levocetirizine Dihydrochloride 2% (NDC 72934-2113). 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

Df (2 End)

Df (2 End)
Side label of a white plastic container for HYDROCORTISONE 2.5% / LEVOCETIRIZINE DIHYDROCHLORIDE 2%, manufactured by Sincerus Florida, LLC. The label includes directions for use, storage instructions, and contact information for reporting adverse reactions with a QR code at the bottom left.*
FDA Label Image

Sad (2113 2 Front)

Sad (2113 2 Front)
Packaging label of HYDROCORTISONE 2.5% / LEVOCETIRIZINE DIHYDROCHLORIDE 2% cream, 30 grams, by Sincerus Florida, LLC. The label features the product name, active ingredients with strengths, and a logo with teal and orange colors. It states the product is a compounded drug made in the USA.*
FDA Label Image

Dd (2113 2 Middle)

Dd (2113 2 Middle)
Label of HYDROCORTISONE 2.5% / LEVOCETIRIZINE DIHYDROCHLORIDE 2% cream showing active ingredients Hydrocortisone USP 2.5% and Levocetirizine Dihydrochloride USP 2%, with inactive ingredients Emulsifix 2% and Suspendisse Cream 93.5%. The label includes manufacturing date 01/01/1970 and lot number 351025ABCDEFG@1. The product is by Sincerus Florida, LLC and marked Rx only.*

* 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.