Niacinamide 4% / Spironolactone 5%
Product Images NDC 72934-1157

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 Niacinamide 4% / Spironolactone 5% (NDC 72934-1157). 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

S (2 End)

S (2 End)
Side label of a NIACINAMIDE 4% / SPIRONOLACTONE 5% topical product from Sincerus Florida, LLC. The label includes usage directions, contact information for reporting adverse reactions, and storage instructions advising controlled room temperature (20-25°C). The label features a QR code at the bottom.*
FDA Label Image

S (1157 2 Front)

S (1157 2 Front)
Packaging label of NIACINAMIDE 4% / SPIRONOLACTONE 5% gel in a 30 gm container from Sincerus Florida, LLC. The label displays the NDC number 72934-1157-2 and notes the product is a compounded drug made in the USA. The label also features the Sincerus Florida logo in teal and orange.*
FDA Label Image

D (1157 2 Middle)

D (1157 2 Middle)
NIACINAMIDE 4% / SPIRONOLACTONE 5% topical gel container label showing active and inactive ingredients. Active ingredients listed are Niacinamide USP 4% and Spironolactone USP 5%. Inactive ingredients include Glycerin USP, Lavender Oil, and Suspendisse Gel. The label also shows the lot number, manufacturing date, and expiration date (BUD). 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.