Ivermectin 1% / Metronidazole 1% / Niacinamide 4%
Product Images NDC 72934-1131

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 Ivermectin 1% / Metronidazole 1% / Niacinamide 4% (NDC 72934-1131). 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

1131 2 Ingredients

1131 2 Ingredients
The label on a white cylindrical container shows active ingredients: Ivermectin USP 1%, Metronidazole USP 1%, and Niacinamide USP 4%. Inactive ingredients include Butylated Hydroxytoluene NF (BHT) 0.1%, Glycerin USP 10%, Krisgel 100 3%, Potassium Azeloyl Diglycinate 50%, and Suspensisse Gel 32.5%. The product is labeled Rx only with a BUD date of 01/27/2021 and manufactured by Sincerus Florida, LLC.*
FDA Label Image

R (1131 2 End)

R (1131 2 End)
The image shows a white cylindrical container with a label featuring usage directions for IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4% topical product by Sincerus Florida, LLC. Directions include application as directed by a physician, external use only, washing hands after use, and storage at controlled room temperature. Contact information for reporting adverse reactions and a QR code are also visible on the label.*
FDA Label Image

X (1131 2 Front)

X (1131 2 Front)
Ivermectin 1% / Metronidazole 1% / Niacinamide 4% gel in a 30 gm container by Sincerus Florida, LLC. The white bottle label includes the product NDC 72934-1131-2 and indicates it is a compounded drug made in the USA.*

* 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.