Proclearz Solution
Product Images NDC 29784-181

View Photos of 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 Proclearz (NDC 29784-181). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rooftop Consumer Health, Inc., 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

Updated Outer Box (30ml Us Made Box)

Updated Outer Box (30ml Us Made Box)
This is a description of a fast-drying antifungal liquid with 1% Tolnaftate as the active ingredient that is both effective in treating and preventing fungal infections on the toes and fingers on the skin around, adjacent, and under nails. The product comes in a 1FL 0Z (30 mL) bottle with an applicator brush for easy access to affected areas.*
FDA Label Image

Drug Facts Panel (30ml Us Made Drug Facts)

Drug Facts Panel (30ml Us Made Drug Facts)
This is a drug information label for an antifungal liquid that contains 1% tolnaftate and vitamin E. It is indicated for curing athlete's foot and ringworm, preventing recurrent athlete's foot, and relieving itching, scaling, cracking, burning, and redness. The product is flammable and for external use only. It should not be used on children under two years old without consulting a doctor. In case of contact with eyes, rinse thoroughly with water. It is necessary to stop using it if irritation occurs or if there is no improvement within four weeks. The product should be stored at room temperature, between 15°C and 30°C. The inactive ingredients include Aloe Vera gel, propylene glycol, and water. No further information is available due to errors.*
FDA Label Image

Upated Inner Label (30ml Us Made Inner Label)

Upated Inner Label (30ml Us Made Inner Label)
This is a warning label and instructions for the use of a liquid anti-fungal solution called "Active Ingredient Tolnaftate 19%". It is meant for external use only, and caution must be exercised to keep it away from children, fire, and eyes. The product should be shaken well before use, and applied thinly to the affected area twice daily or as directed by a doctor. The user is advised to seek medical attention if irritation persists or if there is no improvement within four weeks. In case of accidental ingestion, medical help should be sought immediately. The product should be stored in its original carton for complete drug facts information, and for questions or comments, PROFOOT, Inc. can be contacted via email or phone. The product is made in the USA.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.