Rugby Tolnaftate 1% Powder

Manufacturer
Rugby Laboratories
Effective date
2025-11-25
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
monthly-update
Hydrated at
2026-06-03 17:40:45

Label at a glance#

ProductRugby Tolnaftate 1% Powder
Active ingredientTOLNAFTATE
Label structure9 sections

Indications and uses

. For effective treatment of most athlete's foot (tinea pedis), and ringworm (tinea corporis) . Relieves itching, scaling, irritation, and discomfort . Clears up most athlete's foot infection and helps keep it from coming back with daily use

Dosage and administration

. Shake well before using . Clean the affected area and dry thoroughly . Apply a thin layer of product over the affected area twice a day (morning and night) or as directed by a doctor . Supervise children in the use of this product . This product is not effective on the scalp or nails . Use daily for 4 weeks . Pay special attention to the spaces between the toes . Wear well-fitting ventilated shoes . Change shoes...

Storage and handling

Store between 2°-30ºC (36°-86°F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

. For effective treatment of most athlete's foot (tinea pedis), and ringworm (tinea corporis)

. Relieves itching, scaling, irritation, and discomfort

. Clears up most athlete's foot infection and helps keep it from coming back with daily use

Warnings

WARNINGS SECTION

For External Use Only

Do not use

OTC - DO NOT USE SECTION

On children under 2 years of age

When using this product

OTC - WHEN USING SECTION

Avoid contact with the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

. Irritation occurs

. There is no improvement within 4 weeks

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

Directions

DOSAGE & ADMINISTRATION SECTION

. Shake well before using

. Clean the affected area and dry thoroughly

. Apply a thin layer of product over the affected area twice a day (morning and night) or as directed by a doctor

. Supervise children in the use of this product

. This product is not effective on the scalp or nails

For Athlets's Foot

DOSAGE & ADMINISTRATION SECTION

. Use daily for 4 weeks . Pay special attention to the spaces between the toes

. Wear well-fitting ventilated shoes . Change shoes and socks at least once daily

. To prevent athlete's foot: clean the feet and dry thoroughly, apply once or twice daily

For Ringworm

DOSAGE & ADMINISTRATION SECTION

Use daily for 4 weeks

Other Information

STORAGE AND HANDLING SECTION

Store between 2°-30ºC (36°-86°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Talc, Corn Starch

Questions and Comments?

OTC - QUESTIONS SECTION

1-800-645-2158

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CR-371081 IN MASTERCR-371081 IN MASTER

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0536-1329-26GM - Gram0536-13293fe28104-1f3e-4670-954c-00bd1c07c94212021-09-07

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0536-13290536-1329-26

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
TOLNAFTATE06KB629TKVACTIB
TALC7SEV7J4R1UIACT
STARCH, CORNO8232NY3SJIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4a8f01ca-10c6-7a6f-e063-6294a90a33fcbe71b8a6-3a5f-0be9-e053-2a95a90a1c402026-02-11WarningsExact identifier
spl set id: be71b8a6-3a5f-0be9-e053-2a95a90a1c40

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.