011218 Niacinamide 2% / Spironolactone 5% / Tretinoin 0.025%
Product Images NDC 72934-1206

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 011218 Niacinamide 2% / Spironolactone 5% / Tretinoin 0.025% (NDC 72934-1206). 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

W (2 End)

W (2 End)
A cylindrical white plastic bottle with a label containing directions for use of 011218 NIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.025%, produced by Sincerus Florida, LLC. The label indicates it is for external use only, advises to wash hands after use, and to apply topically as directed by a physician. It also provides contact information for Sincerus Florida LLC in Pompano Beach, FL, and instructions to report adverse reactions to the FDA.*
FDA Label Image

X (1206 2 Front)

X (1206 2 Front)
Front label of 011218 Niacinamide 2% / Spironolactone 5% / Tretinoin 0.025% gel in a white cylindrical container. The label includes the NDC number 72934-1206-2, active ingredient concentrations, the 30gm gel volume, and the Sincerus Florida, LLC logo. The label states it is a compounded drug made in the USA.*
FDA Label Image

Sf (1206 2 Middle)

Sf (1206 2 Middle)
The image shows a partial view of a white container with a label listing active and inactive ingredients. Active ingredients include Niacinamide USP 2%, Spironolactone USP 5%, and Tretinoin USP 0.025%. Inactive ingredients include Ascorbyl Palmitate FCC, Butylated Hydroxytoluene NF (BHT) 0.2%, Glycerin and Artificial Rose Water, and Sodium Metabisulfite NF 1%. The label also notes the product is prescription-only and includes a lot number and manufacturer contact details. The labeler is Sincerus Florida, LLC.*

* 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.