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Active ingredient

Manufacturer
Dongguan Youmi Trading Co., Ltd
Effective date
2026-05-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-zip
Hydrated at
2026-05-27 18:02:34

Label at a glance#

ProductKDMAN
Active ingredientTOLNAFTATE
Label structure11 sections

Indications and uses

Cures athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). Relieves itching, burning, cracking and discomfort which accompany these conditions. Provides fast relief of skin irritation and odor.

Dosage and administration

Use twice daily (morning and night) during a shower or bath, or as directed by a doctor. Apply the soap to the body and feet, gently massaging over the entire skin. Pay special attention to spaces between the toes and areas prone to odor or skin irritation. For best results, allow the lather to remain on the skin for 1 to 2 minutes before rinsing. Rinse and dry the skin and feet thoroughly. Supervise children in t...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

  • Cures athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis).
  • Relieves itching, burning, cracking and discomfort which accompany these conditions.
  • Provides fast relief of skin irritation and odor.

Warnings

WARNINGS SECTION

  • For external use only.

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 eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Irritation occurs.
  • There is no improvement within 4 weeks for athlete's foot or ringworm, or 2 weeks for jock itch.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

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

  • Use twice daily (morning and night) during a shower or bath, or as directed by a doctor.
  • Apply the soap to the body and feet, gently massaging over the entire skin.
  • Pay special attention to spaces between the toes and areas prone to odor or skin irritation.
  • For best results, allow the lather to remain on the skin for 1 to 2 minutes before rinsing.
  • Rinse and dry the skin and feet thoroughly.
  • Supervise children in the use of this product.
  • For athlete's foot and ringworm: use daily for 4 weeks. For jock itch: use daily for 2 weeks.
  • This product is not effective on the scalp or nails.

Other information

OTHER SAFETY INFORMATION

  • Store at room temperature 15°-30°C (59°-86°F).
  • Protect from excessive moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

SORBITOL, SUCROSE, STEARIC ACID, AQUA, PROPYLENE GLYCOL, GYLVCERIN, SODIUM LAURYL SULFATE, COCOS NUCIFERA (COCONUT) OIL, PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL, LAURIC ACID, SODIUM HYDROXIDE, PARFUM, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL

Questions?

OTC - QUESTIONS SECTION

a8888r@outlook.com

Box Front Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KDMAN
TEA TREE OIL ANTIFUNGAL SOAP
6x FAST RELIEVES

Antifungal / Fast Relief
1% Tolnaftate WITH TEA TREE OIL
Net Weight: 2 x 100g

Packaging imagePackaging image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2689792tolnaftate 1 % Medicated Liquid SoapPSN1
2689792tolnaftate 10 MG/ML Medicated Liquid SoapSCD1
2689792tolnaftate 1 % Medicated Liquid SoapSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87723-6625-1KDMAN200 g in 1 BOXSOAP2001

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87723-662587723-6625-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL66YXD4DKO9IACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
COCOS NUCIFERA (COCONUT) OILQ9L0O73W7LIACT
SORBITOL506T60A25RIACT
SUCROSEC151H8M554IACT
STEARIC ACID4ELV7Z65APIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
LAURIC ACID1160N9NU9UIACT
TOLNAFTATE06KB629TKVACTIB
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OILVIF565UC2GIACT
FRAGRANCE 135765EM498GW35IACT
SODIUM LAURYL SULFATE368GB5141JIACT

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
KDMANTOLNAFTATEDongguan Youmi Trading Co., Ltd52a4e836-2059-a49f-e063-6394a90a65562026-05-25WarningsExact identifier
ndc (package): 87723-6625-1
ndc (product): 87723-6625
ndc11 (package): 87723662501
spl id: 52a4e836-205a-a49f-e063-6394a90a6556
spl set id: 52a4e836-2059-a49f-e063-6394a90a6556

Reported adverse events (FAERS/openFDA)#

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