Fungicure Anti-Fungal Wash

Manufacturer
Kobayashi Healthcare International, Inc. | Kobayashi America Manufacturing, LLC
Effective date
2026-10-30
Label type
HUMAN OTC DRUG LABEL
Version
13
Source
monthly-update
Hydrated at
2026-07-17 21:34:14

Label at a glance#

ProductFungicure Anti-Fungal Wash
Active ingredientSEPIA OFFICINALIS JUICE
Label structure13 sections

Indications and uses

For the treatment of most jock itch (tinea cruris) ringworm (tinea corporis) athlete's foot (tinea pedis) tinea versicolor For relief of: itching scaling cracking burning redness soreness irritation discomforts which may accompany these conditions.

Dosage and administration

Read all package directions and warnings before use. Use only as directed. Clean the affected area with Fungicure Anti-Fungal Wash and warm water, rinse and dry thoroughly. For best results, leave on for 1-2 minutes before rinsing and drying. Use twice daily (morning and night), or as directed by a doctor. This product is not effective on scalp or nails. For jock itch, use daily for 2 weeks. For ringworm, tinea ve...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sepia 12x

Purpose

OTC - PURPOSE SECTION

Antifungal treatment

Uses

INDICATIONS & USAGE SECTION

For the treatment of most

  • jock itch (tinea cruris)
  • ringworm (tinea corporis)
  • athlete's foot (tinea pedis)
  • tinea versicolor

For relief of:

  • itching
  • scaling
  • cracking
  • burning
  • redness
  • soreness
  • irritation
  • discomforts which may accompany these conditions.

Warnings

WARNINGS SECTION

For external use only

OTC - ASK DOCTOR SECTION

Ask a doctor before use on children under 2 years of age.

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes.  If contact occurs rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation occurs
  • there is no improvement within 2 weeks (4 weeks for ringworm, athlete's foot and tinea versicolor).

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  If swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Read all package directions and warnings before use.
  • Use only as directed.
  • Clean the affected area with Fungicure Anti-Fungal Wash and warm water, rinse and dry thoroughly.
  • For best results, leave on for 1-2 minutes before rinsing and drying.
  • Use twice daily (morning and night), or as directed by a doctor.
  • This product is not effective on scalp or nails.
  • For jock itch, use daily for 2 weeks.
  • For ringworm, tinea versicolor and athlete's foot, use daily for 4 weeks. If condition persists longer, consult 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.
  • Intended for use by normally healthy adults only.
  • Persons under 18 years of age or those with highly sensitive or allergic skin should use only as directed by a doctor.
  • Supervise children in the use of this product.

Other information

INFORMATION FOR PATIENTS SECTION

You may report serious side effects to the phone number provided under Questions? below.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Lauramidopropyl betaine, panthenol, phospholipid EFA, purified water, sodium chloride, sodium C14 - 16 olefin sulfonate, tea tree oil.

OTC - QUESTIONS SECTION

Questions?  1-800-792-2582

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130072959265069GTIN-13: 0072959265069
EAN-13: 0072959265069
GTIN-12: 072959265069
UPC-A: 072959265069
GTIN storage (14 digits): 00072959265069
T26-10RAP.jpg
QR code linkQR Codebit.ly/4oUUI88?r=qrT26-10RAP.jpg

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SEPIA OFFICINALIS JUICEACTIVE INGREDIENTQDL83WN8C23
SEPIA OFFICINALIS JUICEACTIVE MOIETYQDL83WN8C23
Lauramidopropyl betaineINACTIVE INGREDIENT23D6XVI2333
Lecithin, soybeanINACTIVE INGREDIENT1DI56QDM623
PanthenolINACTIVE INGREDIENTWV9CM0O67Z3
Sodium C14-16 olefin sulfonateINACTIVE INGREDIENTO9W3D3YF5U3
Sodium chlorideINACTIVE INGREDIENT451W47IQ8X3
TEA TREE OILINACTIVE INGREDIENTVIF565UC2G3
WaterINACTIVE INGREDIENT059QF0KO0R3

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
52389-22652389-226-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
112025-04-11full-release2026-06-01 02:33:14

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 16 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62CAPSULE / ORAL20 mgExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62CAPSULE / ORAL20 mgExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62TABLET, FILM COATED / ORAL0.33 mgExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62TABLET, FILM COATED / ORAL0.33 mgExact identifier — unii candidate
14 equally ranked IID candidates
Sodium chlorideSODIUM CHLORIDE451W47IQ8XSOAP / TOPICAL1.26 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62AEROSOL, METERED / RESPIRATORY (INHALATION)0.1 %w/wExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62TABLET, EXTENDED RELEASE / ORAL20 mgExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62TABLET, EXTENDED RELEASE / ORAL20 mgExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62TABLET / ORAL8 mgExact identifier — unii candidate
14 equally ranked IID candidates
Sodium chlorideSODIUM CHLORIDE451W47IQ8XSOAP / TOPICAL1.26 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62TABLET / ORAL8 mgExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62CREAM / VAGINAL1 %w/wExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62CREAM / VAGINAL1 %w/wExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62POWDER, FOR SUSPENSION / ORAL39 mgExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62AEROSOL, METERED / RESPIRATORY (INHALATION)0.1 %w/wExact identifier — unii candidate
14 equally ranked IID candidates
Lecithin, soybeanSOYBEAN LECITHIN1DI56QDM62POWDER, FOR SUSPENSION / ORAL39 mgExact identifier — unii candidate
14 equally ranked IID candidates

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
Fungicure Anti-Fungal WashSEPIAKobayashi Healthcare International, Inc.ba0cea2d-23ee-4725-abcf-72a62ad581762026-10-30WarningsExact identifier
ndc (package): 52389-226-06
ndc (product): 52389-226
ndc11 (package): 52389022606
spl id: 5517de4d-43c6-82d3-e063-6394a90ab351
spl set id: ba0cea2d-23ee-4725-abcf-72a62ad58176

Reported adverse events (FAERS/openFDA)#

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