Drugplain

Tolnaftate 1.3 g/113g

Foot Odor Control Powder Spray · AEROSOL, SPRAY · Winco Foods, LLC

10 Recalls on Record
Plain English

Tolnaftate is an over-the-counter spray powder applied to the skin to help control foot odor. It comes as an aerosol spray that you apply directly to your feet.

Key Facts

Brand Name
Tolnaftate
Generic Name
Foot Odor Control Powder Spray
NDC Code (Product)
67091-390
Manufacturer
Winco Foods, LLC
Strength
1.3 g/113g
Dosage Form
AEROSOL, SPRAY
Route
TOPICAL
Marketing Status
Application #
M005
Marketing Start
09/29/2021

Recall History

10 Recalls on Record
Class I10/01/2021

Bayer Healthcare Pharmaceuticals Inc.

Chemical Contamination: presence of benzene

TerminatedVoluntary: Firm initiated
Class I10/01/2021

Bayer Healthcare Pharmaceuticals Inc.

Chemical Contamination: presence of benzene

TerminatedVoluntary: Firm initiated
Class II10/01/2021

Bayer Healthcare Pharmaceuticals Inc.

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

TerminatedVoluntary: Firm initiated
Class I10/01/2021

Bayer Healthcare Pharmaceuticals Inc.

Chemical Contamination: presence of benzene

TerminatedVoluntary: Firm initiated
Class II10/01/2021

Bayer Healthcare Pharmaceuticals Inc.

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

TerminatedVoluntary: Firm initiated
Class II10/01/2021

Bayer Healthcare Pharmaceuticals Inc.

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

TerminatedVoluntary: Firm initiated
Class I10/01/2021

Bayer Healthcare Pharmaceuticals Inc.

Chemical Contamination: presence of benzene

TerminatedVoluntary: Firm initiated
Class II10/01/2021

Bayer Healthcare Pharmaceuticals Inc.

cGMP Deviations: LOTRIMIN AF (Tolnaftate 1%) manufactured at the same facility where other lots were found to be contaminated with benzene.

TerminatedVoluntary: Firm initiated
Class II08/09/2023

Ecometics, Inc.

CGMP Deviations: Products not manufactured under current good manufacturing practices.

CompletedVoluntary: Firm initiated
Class II10/01/2021

Bayer Healthcare Pharmaceuticals Inc.

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

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

arthralgia17 reports
diarrhoea16 reports
headache13 reports
rash erythematous13 reports
blood potassium increased12 reports
fatigue12 reports
bronchopulmonary aspergillosis11 reports
dyspnoea11 reports
mucormycosis11 reports
off label use11 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses proven clinically effective in the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis) prevent recurrence of most athlete's foot with daily use for effective relief of itching, cracking and burning

Dosage & Administration

Directions wash affected area and dry thoroughly shake can well and spray 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 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, consult a doctor to prevent athlete's foot: wash the feet and dry thoroughly; spray a thin layer of the product to the feet once or twice daily (morning and/or night) this product is not effective on the scalp or nails if nozzle clogs, clean with a pin

Warnings

Warnings For external use only. Flammable: Contents under pressue. Avoid spraying in eyes. Do not use or store near heat or open flame. Do not puncture or incinerate container. Do not store at temperature above 120F. Keep out of reach of children. Use only as directed. Intentional misuse by dilberately concentrating and inhaling the contents can be harmful or fatal. When using this product avoid contact with the eyes or mouth use only as directed Stop use and ask a doctor if irritation occurs no improvement within 4 weeks for athlete's foot and ringworm Do not use on children under 2 years of age unless directed by a doctor. Keep out of reach od children. If swallowed, get medical hel or contact a Poison Control Center right away.

Frequently Asked Questions

What is Tolnaftate used for?

Tolnaftate is an over-the-counter spray powder applied to the skin to help control foot odor. It comes as an aerosol spray that you apply directly to your feet.

Is Tolnaftate a controlled substance?

Tolnaftate is not classified as a controlled substance by the DEA.

What is the generic name for Tolnaftate?

The generic name for Tolnaftate is Foot Odor Control Powder Spray. There are 1 other brand versions of Foot Odor Control Powder Spray.

What is the NDC code for Tolnaftate 1.3 g/113g?

The NDC (National Drug Code) for Tolnaftate 1.3 g/113g is 67091-390, listed by Winco Foods, LLC.

Product NDC

67091-390

Package NDC

67091-390-04

Other Tolnaftate Dosages

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

Data from openFDA · Public domain (CC0 1.0)