Dermatool Fungal Nail Treatment 1 g/100mL

Tolnaftate 1% · LIQUID · Papalo Group LLC

No Recall History

Plain English

Dermatool Fungal Nail Treatment is a liquid containing tolnaftate 1% at 1 g/100mL, taken topical. Manufactured by Papalo Group LLC.

Key Facts

Brand Name: Dermatool Fungal Nail Treatment
Generic Name: Tolnaftate 1%
NDC Code (Product): 84728-510
Manufacturer: Papalo Group LLC
Strength: 1 g/100mL
Dosage Form: LIQUID
Route: TOPICAL
Marketing Status
Application #: M005
Marketing Start: 04/06/2023

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective1 reports

muscular weakness1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Cures most Athlete's Foot (Tinea Pedis) and Ringworm (Tinea Corporis). Relieves itching, scaling, cracking, burning, redness, sorenes, and irritation and discomfort. Helps prevent most athlete's foot (dermatophytosis) with daily use.

Dosage & Administration

For athlete's foot and ringworm: use daily for 4 weeks. Clean the affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Supervise children in the use of this product. This product is not effective for the treatment of ringworm of the scalp or nails. For athlete's foot: pay special attention to spaces between the toes, wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. To prevent athlete's foot, apply once or twice daily (morning and/or night). Apply to skin around the nail and cuticle.

Warnings

For external use only. Do not use on children under 2 years of age unless directed by a doctor. When using this product avoid contact with eyes. Stop use and ask a doctor if: irritation occurs, there is no improvement within 4 weeks (for athlete's foot and ringworm).

Frequently Asked Questions

What is Dermatool Fungal Nail Treatment used for?

Dermatool Fungal Nail Treatment contains Tolnaftate 1%. It is a liquid taken topical. Consult your doctor for specific uses.

Is Dermatool Fungal Nail Treatment a controlled substance?

Dermatool Fungal Nail Treatment is not classified as a controlled substance by the DEA.

What is the generic name for Dermatool Fungal Nail Treatment?

The generic name for Dermatool Fungal Nail Treatment is Tolnaftate 1%. There are 12 other brand versions of Tolnaftate 1%.

What is the NDC code for Dermatool Fungal Nail Treatment 1 g/100mL?

The NDC (National Drug Code) for Dermatool Fungal Nail Treatment 1 g/100mL is 84728-510, listed by Papalo Group LLC.

Product NDC

84728-510

Package NDC

84728-510-01

Other Tolnaftate Brands

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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)