Active ingredient

Manufacturer
Nanjing Qiaotun Technology Co., Ltd.
Effective date
2026-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-18 05:11:30

Label at a glance#

ProductOAKDOLCHE Tea Tree Oil Antifungal
Active ingredientTOLNAFTATE
Label structure10 sections

Indications and uses

For the cure of most athlete's foot, jock itch, and ringworm. Relieves itching, burning, cracking, and scaling associated with these conditions.

Dosage and administration

Wet affected area and lather with soap. Wash affected area and dry thoroughly. Use twice daily, morning and night, or as directed by a doctor. 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. Use daily for 4 weeks for athlete's foot and ringworm, or 2 weeks for jock itch. Children under 2 years of age: ask a do...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

For the cure of most athlete's foot, jock itch, and ringworm.

Relieves itching, burning, cracking, and scaling associated with these conditions.

Warnings

WARNINGS SECTION


For external use only.
Do not use on children under 2 years of age unless directed by a doctor.
When using this product avoid contact with the eyes.
Stop use and ask a doctor if irritation occurs or if there is no improvement within 4 weeks for athlete's foot or ringworm, or within 2 weeks for jock itch.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet affected area and lather with soap.

Wash affected area and dry thoroughly.

Use twice daily, morning and night, or as directed by a doctor.

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.

Use daily for 4 weeks for athlete's foot and ringworm, or 2 weeks for jock itch.

Children under 2 years of age: ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sodium Laureth Sulfate, Stearic Acid, Propylene Glycol, Sorbitol, Sucrose, Lauric Acid, Glycerin, Water, Sodium Hydroxide, Olea Europaea (Olive) Fruit Oil, Cocos Nucifera (Coconut) Oil, Butyrospermum Parkii (Shea) Butter, Centella Asiatica Whole, Melaleuca Alternifolia (Tea Tree) Leaf, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Sophora Flavescens Root, Titanium Dioxide, Edetate Disodium.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Other information

OTHER SAFETY INFORMATION

Store at 20° to 25°C (68° to 77°F).
Avoid excessive heat and moisture.

Questions?

OTC - QUESTIONS SECTION

Questions? Contact Nanjing Qiaotun Technology Co., Ltd.

Email: qiaotljh@163.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OAKDOLCHE Tea Tree Oil Antifungal Soap

Active ingredient: Tolnaftate 1%

NDC 87864-001-01

Net Wt. 5 × 80 g (400 g / 14 oz)

Tea Tree Oil Antifungal SoapTea Tree Oil Antifungal Soap

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87864-00187864-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
OAKDOLCHE Tea Tree Oil AntifungalTOLNAFTATENanjing Qiaotun Technology Co., Ltd.569dee15-e68d-220e-e063-6294a90af7c52026-07-14WarningsExact identifier
ndc (package): 87864-001-01
ndc (product): 87864-001
ndc11 (package): 87864000101
spl id: 569dee15-e68e-220e-e063-6294a90af7c5
spl set id: 569dee15-e68d-220e-e063-6294a90af7c5

Reported adverse events (FAERS/openFDA)#

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