FDA.reportPublic FDA data

Rugby Athlete's Foot Powder Spray Tolnaftate 1%

Manufacturer
Rugby Laboratories
Effective date
2026-05-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
weekly-update
Hydrated at
2026-07-17 21:43:30

Label at a glance#

ProductAthletes Foot
Active ingredientTOLNAFTATE
Label structure10 sections

Indications and uses

cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris) helps prevent most athlete's foot with daily use relieves itching, burning, cracking, and chafing associated with jock itch

Dosage and administration

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 to prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or night) supervise children in the use of this product for athlete's foot: pay special attention to spaces between the toe...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • cures most athlete's foot (tinea pedis), ringworm (tinea corporis) and jock itch (tinea cruris)
  • helps prevent most athlete's foot with daily use
  • relieves itching, burning, cracking, and chafing associated with jock itch

Warnings

WARNINGS SECTION

For external use only.

Extremely Flammable:

SAFE HANDLING WARNING SECTION

Keep away from fire, sparks, and heated surfaces. Contents under pressure. Do not puncture or incinerate. Do not store at
temperature above 120°F.

Do not use

OTC - DO NOT USE SECTION

on children under 2 years of age unless directed by a doctor.

When using this product

OTC - WHEN USING SECTION

  • avoid spraying in eyes
  • use only as directed
  • intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • there is no improvement within 4 weeks for athlete's foot and ringworm; 2 weeks for jock itch
  • irritation occurs

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

  • 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
  • to prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or night)
  • 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; for jock itch, use daily for 2 weeks
  • if condition persists, consult a doctor
  • this product is not effective on the scalp or nails

Other information

OTHER SAFETY INFORMATION

  • store between 20º and 30ºC (68º and 86ºF)
  • if nozzle clogs, clean with a pin

Inactive ingredients

INACTIVE INGREDIENT SECTION

ISOBUTANE, SD ALCOHOL 40-B, KAOLIN, ZEA MAYS (CORN) STARCH, BHT, PPG-12-BUTETH-16

Questions?

OTC - QUESTIONS SECTION

Call 1-866-964-0939

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by Bayer HealthCare LLC, owner of the registered trademark Tinactin®.

Distributed by:
RUGBY LABORATORIES,
Indianapolis, IN 46268
(800) 616-2471
www.major-rugby.com

Rev. 04/26 R-192 Re-order No. 371280

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0536-1481-01

rugby

athlete's foot
powder spray

tolnaftate 1%
antifungal

  • cures most athlete's foot &

prevents recurrences

  • relieves itching, cracking

& burning

  • comforts & refreshes
  • talc-free

net wt. 4.6 oz. (130 g)

cartoncarton

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0536-14810536-1481-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ISOBUTANEBXR49TP611IACT
KAOLIN24H4NWX5COIACT
PPG-12-BUTETH-1658CG7042J1IACT
ALCOHOL3K9958V90MIACT
ZEA MAYS SUBSP. MAYS WHOLE1G5HNE09V8IACT
TOLNAFTATE06KB629TKVACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-05-14full-release2026-06-01 01:57:31
12026-05-06weekly-update2026-06-03 18:02:42

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
Athletes FootTOLNAFTATERugby Laboratories50c46cf5-3e64-9e0f-e063-6294a90a23172026-05-14WarningsExact identifier
ndc (package): 0536-1481-01
ndc (product): 0536-1481
ndc11 (package): 00536148101
spl id: 51cff2fc-39c4-3a1a-e063-6294a90aeea5
spl set id: 50c46cf5-3e64-9e0f-e063-6294a90a2317

Reported adverse events (FAERS/openFDA)#

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