Imiquimod 5% / Tretinoin 0.025%
Product Images NDC 72934-1129

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% / Tretinoin 0.025% (NDC 72934-1129). 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

Wr (2 End)

Wr (2 End)
Side view of a white plastic container for IMIQUIMOD 5% / TRETINOIN 0.025%, labeled by Sincerus Florida, LLC. The label includes directions for use, advising to apply topically as directed by a physician and to wash hands after use, with a storage temperature of 20-25°C. Contact information for the manufacturer and FDA adverse reaction reporting details are also visible.*
FDA Label Image

Ca (1129 2 Front)

Ca (1129 2 Front)
Packaging label for IMIQUIMOD USP 5% / TRETINOIN USP 0.025% gel in a 30 gram container. The label includes the NDC 72934-1129-2 and the name of the labeler, Sincerus Florida, LLC. The label also states that this is a compounded drug made in the USA.*
FDA Label Image

Dw (1129 2 Middle)

Dw (1129 2 Middle)
Side view of a white cylindrical container label for IMIQUIMOD 5% / TRETINOIN 0.025% gel by Sincerus Florida, LLC. The label lists active ingredients Imiquimod USP 5% and Tretinoin USP 0.025%, and inactive ingredients Glycerin USP 5% and Suspendisse Gel 89.675%. It also shows manufacturing and expiration dates along with lot number details.*

* 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.