071023 Econazole Nitrate 1% / Niacinamide 4%
Product Images NDC 72934-2218

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 071023 Econazole Nitrate 1% / Niacinamide 4% (NDC 72934-2218). 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

De (2 End)

De (2 End)
071023 ECONAZOLE NITRATE 1% / NIACINAMIDE 4% in a white plastic container with a label showing usage directions and contact information for Sincerus Florida, LLC. Directions instruct external use, applying topically as directed by a physician and washing hands after use. The label includes storage instructions at controlled room temperature and company contact details.*
FDA Label Image

Df (2218 2 Front)

Df (2218 2 Front)
071023 ECONAZOLE NITRATE 1% / NIACINAMIDE 4% cream in a white container with a dispensing cap. The label displays the active ingredients with their strengths, the package size of 30 gm, and the labeler Sincerus Florida, LLC. The label also includes the NDC number 72934-2218-2 and states the product is a compounded drug made in the USA.*
FDA Label Image

Z (2218 2 Middle)

Z (2218 2 Middle)
071023 ECONAZOLE NITRATE 1% / NIACINAMIDE 4% cream in a white cylindrical container. The visible label section lists active ingredients Econazole Nitrate USP 1% and Niacinamide USP 4%, and inactive ingredients comprising 95% of the formulation. The label includes a lot number and placeholders for BUD and manufacturing date, with the labeler name Sincerus Florida, LLC partially visible.*

* 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.