Imiquimod 5% / Levocetirizine Dihydrochloride 1% / Tretinoin 0.05%
Product Images NDC 72934-1011

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 Imiquimod 5% / Levocetirizine Dihydrochloride 1% / Tretinoin 0.05% (NDC 72934-1011). 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

D (1011 2 End)

D (1011 2 End)
Container label of IMIQUIMOD 5% / LEVOCETIRIZINE DIHYDROCHLORIDE 1% / TRETINOIN 0.05%, a topical medication by Sincerus Florida, LLC. The white cylindrical container displays usage directions and manufacturer contact information, including storage instructions to keep at controlled room temperature (20-25°C) and a note that the product is for office use only, not for resale.*
FDA Label Image

';' (1011 2 Front)

';' (1011 2 Front)
A white cylindrical tube labeled with NDC 72934-1011-2 containing a compounded gel formulation with Benzoyl Peroxide USP 2.5%, Clindamycin Phosphate USP 1%, Niacinamide USP 2%, and Tretinoin USP 0.025%, 30 grams. The label includes the Sincerus Florida logo and states that the product is made in the USA.*
FDA Label Image

F (1011 2 Middle)

F (1011 2 Middle)
Drug ingredient panel from IMIQUIMOD 5% / LEVOCETIRIZINE DIHYDROCHLORIDE 1% / TRETINOIN 0.05% shows active ingredients including Benzoyl Peroxide USP 2.5%, Clindamycin Phosphate USP 1%, Niacinamide USP 2%, and Tretinoin USP 0.025%. Inactive ingredients listed include Butylated Hydroxytoluene NF (BHT) 0.1%, Glycerin USP 5%, Lavender Oil 0.25%, and Sodium Metabisulfite NF 0.1%, in a water-based gel suspension.*

* 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.