GoodSense Powder Spray Jock Itch Antifungal Tolnaftate

Manufacturer
Formulated Solutions, LLC
Effective date
2023-12-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:03:24

Label at a glance#

ProductGoodSense Powder Jock Itch Antifungal
Active ingredientTOLNAFTATE
Label structure8 sections

Indications and uses

cures most jock itch for effective relief if itching, chanting and burning

Dosage and administration

wash affected area and dry thoroughly shake can well and spray a thin layer over affected area twice daily (morning and night) supervise children in the use of this product use daily for 2 weeks; if condition persist longer, ask a doctor this product is not effective on the scalp or nails In case of  clogging, clean nozzle with a pin

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • cures most jock itch
  • for effective relief if itching, chanting and burning

Warnings

WARNINGS SECTION

For external use only

Flammable: Do not use while smoking or near heat or flame

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 contact with the eyes
  • use only as directed intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal
  • contents under pressure. Do not punture or incinerate. Do not store at temperature above 120°F (49°C).

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation occurs
  • there is no improvement within 2 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 right away (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

  • wash affected area and dry thoroughly
  • shake can well and spray a thin layer over affected area twice daily (morning and night)
  • supervise children in the use of this product
  • use daily for 2 weeks; if condition persist longer, ask a doctor
  • this product is not effective on the scalp or nails
  • In case of  clogging, clean nozzle with a pin

Other information

SPL UNCLASSIFIED SECTION

store at 20-25°C (68-77°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

alcohol denat, aluminum starch octenylsuccinate, isobutane, isopropyl myristate, propylene carbonate, sorbitan monooleate, stearalkonium hectorite, talc

Questions or comments?

OTC - QUESTIONS SECTION

1-800-719-9260

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Spray 806Spray 806

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
705934tolnaftate 1 % Powder SprayPSN2
705934tolnaftate 0.01 MG/MG Powder SpraySCD2
705934tolnaftate 1 % Powder SpraySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23667-806-01GoodSense Powder Jock Itch Antifungal130 g in 1 CANSPRAY1302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23667-806GOODSENSE POWDER JOCK ITCH ANTIFUNGAL (TOLNAFTATE) SPRAY [FORMULATED SOLUTIONS, LLC]2Legacy NDC, 1 package rows20231207_46c5fa20-1297-272e-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
23667-80623667-806-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
567fd160-80af-f7ac-e063-6394a90a4cf246c5fa20-1297-272e-e054-00144ff8d46c2026-07-13WarningsExact identifier
spl set id: 46c5fa20-1297-272e-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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