Imiquimod 5% / Levocetirizine Dihydrochloride 1% / Tretinoin 0.05%
Product Images NDC 72934-1126

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Imiquimod 5% / Levocetirizine Dihydrochloride 1% / Tretinoin 0.05% (NDC 72934-1126). 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

X (1126 2 End)

Side view of a white plastic container with a label displaying directions for use and manufacturer contact information for IMIQUIMOD 5% / LEVOCETIRIZINE DIHYDROCHLORIDE 1% / TRETINOIN 0.05% by Sincerus Florida, LLC. The label includes instructions to use as directed by a physician, apply topically, wash hands after use, and store at controlled room temperature (20-25°C). Manufacturer contact details and reporting info for adverse reactions are also shown.*

FDA Label Image

X (1126 2 Front)

White cylindrical container labeled with Imiquimod USP 5%, Levocetirizine Dihydrochloride USP 1%, and Tretinoin USP 0.05% in gel form, 30gm. The label includes the NDC 72934-1126-2 and shows the Sincerus Florida, LLC logo in teal and orange. It states that this is a compounded drug made in the USA.*

FDA Label Image

D (1126 2 Middle)

Side view of a white cylindrical container label listing active and inactive ingredients of IMIQUIMOD 5% / LEVOCETIRIZINE DIHYDROCHLORIDE 1% / TRETINOIN 0.05% topical gel. The label includes Imiquimod USP 5%, Levocetirizine Dihydrochloride USP 1%, Tretinoin USP 0.05% as active ingredients, and mentions inactive ingredients such as Krisgel 100, Polysorbate 60 NF, and suspending gel. The label also contains Rx only, lot number, and manufacturing and expiration dates.*

* 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.