Nail Renew Liquid
Product Images NDC 62858-101

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nail Renew (NDC 62858-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nailrenew Corp, 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

Nailrenew_bottlelabel_back-1 (Nailrenew Bottlelabel Back 1)

Drug Facts panel for Nail Renew topical liquid with Tolnaftate 1.0% as the active ingredient. The panel lists uses for fungal skin infections including athlete's foot and ringworm, warnings for external use only, precautions about accidental ingestion and rash, and directions not to use on children under 2 or near eyes, ears, or mouth. Contact email for questions is provided.*

FDA Label Image

Nailrenew_bottlelabel_back-2 (Nailrenew Bottlelabel Back 2)

A directions and inactive ingredients panel for NAIL RENEW topical liquid. Directions instruct cleaning the affected area, applying 2-3 drops twice daily to nails and surrounding skin, allowing solution to soak or dry, noting ineffectiveness on scalp or nails, recommending application to adjacent fingers or toes to prevent spread, and hygiene to prevent reinfection. Inactive ingredients include water, PEG-8, glyceryl stearate, cetearyl alcohol, and others.*

FDA Label Image

Nailrenew_bottlelabel_front (Nailrenew Bottlelabel Front)

Label for NAIL RENEW fungal renewal solution, a topical liquid OTC drug containing Tolnaftate at 1 g/100 mL. The label shows the brand name 'NailRENEW Professional Strength' and indicates the packaging size as 1 FL OZ (30 mL). It includes the website nail-renew.com and is labeled by Nailrenew Corp.*

* 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.