Tolfyra .3 g/30mL
Tolnaftate · LIQUID · Oncora Pharma, LLC
Tolfyra is a liquid containing tolnaftate at .3 g/30mL, taken topical. Manufactured by Oncora Pharma, LLC.
Key Facts
- Brand Name
- Tolfyra
- Generic Name
- Tolnaftate
- NDC Code (Product)
85477-331- Manufacturer
- Oncora Pharma, LLC
- Strength
- .3 g/30mL
- Dosage Form
- LIQUID
- Route
- TOPICAL
- Marketing Status
- Application #
- M005
- Marketing Start
- 05/01/2026
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Uses ■ for the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis). ■ relieves itching, burning, cracking, scaling, and discomfort which accompany these conditions. ■ for the prevention of most Athlete’s foot with daily use. ■ eliminates fungus on fingers, toes, and around the nails. ■ eliminates and helps stop the spread of fungal infections on cuticles around nail edges and under the nail tips where reachable with applicator brush.
Dosage & Administration
Directions ■ clean the affected area and dry thoroughly ■ apply a thin layer of the product over affected area twice daily (morning and night) paying special attention to the edges of the nail, cuticles, and skin around the nails or as directed by a doctor ■ supervise children in the use of this product ■ 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 ■ for athlete's foot and ringworm, use daily for 4 weeks ■ if condition persists longer, consult a doctor. Use under the direction of a medical practitioner
Warnings
Warnings For external use only Do not use on children under 2 years of age unless directed by a doctor. When using this product ■ do not get into eyes Stop use and ask a doctor ■ for athlete's foot and ringworm - if irritation occurs or there is no improvement within 4 weeks ■ for prevention of athlete’s foot - if irritation occurs, discontinue use and consult a doctor Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Frequently Asked Questions
What is Tolfyra used for?
Tolfyra contains Tolnaftate. It is a liquid taken topical. Consult your doctor for specific uses.
Is Tolfyra a controlled substance?
Tolfyra is not classified as a controlled substance by the DEA.
What is the generic name for Tolfyra?
The generic name for Tolfyra is Tolnaftate. There are 11 other brand versions of Tolnaftate.
What is the NDC code for Tolfyra .3 g/30mL?
The NDC (National Drug Code) for Tolfyra .3 g/30mL is 85477-331, listed by Oncora Pharma, LLC.
Other Tolnaftate Brands
See all →- Tolnaftate Antifungal Powder1 g/100g73469-0619
- Maximum Strength Antifungal Liquid10 mg/mL79481-0660
- Tolnafate10 mg/g83324-234
- Quali Life ANTIFUNGAL CHARCOAL1 g/100g83566-607
- Nailtific Nighttime Antifungal Renewal Pen Refill.06 g/6mL84167-023
- SERYNTH FUNGI NAIL1 g/100mL85248-108
- PUVIDA FUNGAL NAIL1 g/100185248-153
- Tagrid Athletes Foot Treament10 mg/g85384-0008
- Hermon Ringworm Treatment Body Wash5 g/500g85398-028
- Hermon Jock Itch Antifungal Treatment .Soap. Bar1.13 g/113g85398-031
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)