Propedix Dryello Tolnaftate 1% Antifungal Improved (v1b) - 0.53 oz Stick - 2pk

Manufacturer
ProPedix, Inc. | Columbia Cosmetics Manufacturing, Inc.
Effective date
2026-10-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-10 01:03:26

Label at a glance#

ProductDryello Tolnaftate 1% Antifungal
Active ingredientTOLNAFTATE
Label structure9 sections

Indications and uses

Cures most Athlete's Foot (tinea pedis) Relieves itching, burning, cracking, and scaling Prevents recurrence of most Athlete's foot with daily use

Dosage and administration

Wash feet and dry thoroughly. Apply a think layer of the product to the affected area twice daily (morning and night). Supervise children in the use of this product. Pay special attention to spaces between toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.

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)
  • Relieves itching, burning, cracking, and scaling
  • Prevents recurrence of most Athlete's foot with daily use

Warnings

WARNINGS SECTION

Do not use on children under 2 years of age unless directed by a doctor.

For external use only. Avoid contact with eyes.

When using this product

OTC - WHEN USING SECTION

  • If irritation occurs, discontinue use and consult a doctor

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wash feet and dry thoroughly.
  • Apply a think layer of the product to the affected area twice daily (morning and night).
  • Supervise children in the use of this product.
  • Pay special attention to spaces between toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.

Other

OTHER SAFETY INFORMATION

Store between 68º - 86ºF (20º - 30ºC)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aluminum Hydroxide, Arrowroot Powder, Behenyl Behenate, C12-15 Alkyl Benzoate, Cyclopentasiloxane, Magnesium Aluminum Silicate, Magnesium Citrate, Magnesium Hydroxide, Magnesium Sulfate, Orange Peel Oil, Stearyl Alcohol, Tocopheryl Acetate.

Questions?

OTC - QUESTIONS SECTION

1-800-452-7362 dryello.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

For Athlete's Foot

Treats + Prevents

New Silky Smooth Application

Dryello TM

TOLNAFTATE 1% ANTIFUNGAL

Vlinically Proven
Dermatologist Developed

Two Glide-On Sticks

Two 15g (0.53oz) NET WT Sticks

Box Dryello 2pk ImprovedBox Dryello 2pk Improved

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860015318039GTIN-13: 0860015318039
EAN-13: 0860015318039
GTIN-12: 860015318039
UPC-A: 860015318039
GTIN storage (14 digits): 00860015318039
Box Dryello 2pk 20260402 M.jpg
QR code linkQR Codedryello.com/Box Dryello 2pk 20260402 M.jpg

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85565-00585565-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-04-03full-release2026-06-01 01:52:36

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
Dryello Tolnaftate 1% AntifungalTOLNAFTATEProPedix, Inc.4e962ca4-80ee-a379-e063-6394a90a13222026-04-03WarningsExact identifier
ndc (package): 85565-005-01
ndc (product): 85565-005
ndc11 (package): 85565000501
spl set id: 4e962ca4-80ee-a379-e063-6394a90a1322

Reported adverse events (FAERS/openFDA)#

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