Funginix Anti-fungal Treatment Ointment
Product Images NDC 71229-102

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Funginix Anti-fungal Treatment (NDC 71229-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Sisquoc Healthcare Corporation, 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

Funginix Insert (Funginix Insert)

Funginix Insert (Funginix Insert)
Funginix Maximum Strength Anti-Fungal Treatment is a medication designed to treat fungal infections of the skin, particularly those that affect the nails. These infections are caused by many different types of fungi that live in moist, dark conditions and which find their way into small openings in the skin. Funginix is formulated with Undecylenic Acid, an anti-fungal agent that inhibits the growth and spread of fungal cells, effectively destroying the infection. The treatment is intended to be applied twice a day for at least three months in order to achieve maximum results. Funginix acts quickly to eliminate the fungal infection at the site of the infection, making it an effective choice for fungal skin infections. If symptoms persist for more than four weeks, a physician should be consulted.*
FDA Label Image

Funginix Label (Funginix Label)

Funginix Label (Funginix Label)
This is a description of an anti-fungal treatment that contains an active ingredient called rdcyeric Acd at 10%. It is used externally only and should not be used on children under 2 years old without doctor's direction. It should be shaken well before use and applied twice a day to the affected area. It is important not to get it in contact with the eyes, but if it happens, rinse thoroughly with water. Stop use and seek medical attention if symptoms persist after 4 weeks. The product should be allowed to absorb into the surrounding area for 3-4 minutes. There is additional information included on a drug facts sheet. Distributed by Sisquoc Healthcare, Inc. based in Newport Beach, CA. If swallowed, medical assistance or poison control center should be contacted.*

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