Rmmz Fungal Nail Renewal Set
Product Images NDC 74458-196

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Rmmz Fungal Nail Renewal Set (NDC 74458-196). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guangzhou Yilong Cosmetics.,ltd, 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

1 (20260601181828 26 6835(1)(1))

1 (20260601181828 26 6835(1)(1))
Packaging label for RMMZ Fungal Nail Renewal Set by Guangzhou Yilong Cosmetics.,Ltd. The design features blue and white colors and includes instructions for use, active ingredients Undecylenic acid 25% and Tolnaftate 1%, and product specifications for a topical fungal treatment pen and patches. It lists package components including nail patches and a treatment pen with a 3 ml (0.1 fl oz) volume, and usage directions for fungal nail care. The box has visuals illustrating a step-by-step application process and the label prominently states 'Fungal Nail Renewal'.*
FDA Label Image

5340bba3 8fd6 62f5 E063 6294a90a224c

5340bba3 8fd6 62f5 E063 6294a90a224c
The image shows the packaging label for RMMZ FUNGAL NAIL RENEWAL SET by Guangzhou Yilong Cosmetics Ltd. The label is primarily blue and white with step-by-step application instructions labeled Step 1 Prep, Step 2 Day, and Step 3 Night. The label indicates the product contains 4 fungal nail pens of 3 ml (0.1 fl oz) each with 25% Undecylenic Acid and 1% Toinaflate. Drug facts and usage instructions are printed on the label, along with company information and directions for application.*

* 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.