Niacinamide 2% / Spironolactone 5% / Tretinoin 0.05%
Product Images NDC 72934-1153

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 2% / Spironolactone 5% / Tretinoin 0.05% (NDC 72934-1153). 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

C (1153 2 End)

C (1153 2 End)
Side label on a white container of NIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.05% by Sincerus Florida LLC. The label includes directions for use, storage instructions, contact information for reporting adverse reactions, and a QR code. The label advises to use as directed by a physician, wash hands after use, and store at controlled room temperature (20-25°C).*
FDA Label Image

C (1153 2 Front)

C (1153 2 Front)
NIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.05% gel in a 30 gram white container. The label includes the NDC number 72934-1153-2 and shows it is a compounded drug made in the USA. The labeler is Sincerus Florida LLC, with the company's logo displayed in teal and orange.*
FDA Label Image

C (1153 2 Middle)

C (1153 2 Middle)
Label of NIACINAMIDE 2% / SPIRONOLACTONE 5% / TRETINOIN 0.05% showing active and inactive ingredients. Active ingredients include Niacinamide USP 2%, Spironolactone USP 5%, and Tretinoin USP 0.05%. Inactive ingredients listed are Ascorbyl Palmitate FCC 1%, Butylated Hydroxytoluene NF (BHT) 0.1%, Glycerin and Artificial Rose Water 0.2%, Sodium Metabisulfite NF 5%, and Suspendisse Gel 86.65%. The label also mentions Rx only and includes the lot number, manufacture date, and BUD.*

* 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.