SFEIXE ANTIFUNGAL PEN

Manufacturer
Zhejiang JOOZENA Medical Technology Co., Ltd.
Effective date
2026-02-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:44:12

Label at a glance#

ProductSFEIXE ANTIFUNGAL PEN
Active ingredientUNDECYLENIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

UNDECYLENIC ACID 25%

OTC - PURPOSE SECTION

Cures most Athlete's Foot (Tinea Pedis) and Ringworm(Tinea Corporis). Relieves itching, scaling, cracking, burning,redness, sorenes, and irritation and discomfort.Helpsprevent most athlete's foot (dermatophytosis) with daily use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medical helpor contact a Poison Control Center right away.

WARNINGS SECTION

Warnings
For external use only.
Do not use on children under 2 years of age unless directedby a doctor.
When using this product, avoid contact with eyes.Stop use and ask a doctor if irritation occurs, there is noimprovement within 4 weeks (for athlete's foot andringworm).

INDICATIONS & USAGE SECTION

This product is not effective for thetreatment of ringworm of the scalp or nails. For athlete's foot:pay special attention to spaces between the toes, wearwell-fitting, ventilated shoes, and change shoes and socks atleast once daily. To prevent athlete's foot, apply once ortwice daily(morning and/or night). Apply to skin around thenail and cuticle.

DOSAGE & ADMINISTRATION SECTION

For athlete's foot and ringworm: use daily for 4 weeks, Cleanthe affected area and dry thoroughly. Apply a thin layer ofthe product over affected area twice daily (morning andnight) or as directed by a doctor. Supervise children in theuse of this product,

INACTIVE INGREDIENT SECTION

water, euphorbia hirta whole, glycerin,hydracrylic acid,pseudolarix amabilis bark, resorcinol,

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87259-001-01SFEIXE ANTIFUNGAL PEN6 mL in 1 TUBEPASTE62
87259-001-01SFEIXE ANTIFUNGAL PEN3 in 1 BOXPASTE32

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87259-00187259-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-12-07monthly-update2026-06-03 17:45:31

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
SFEIXE ANTIFUNGAL PENUNDECYLENIC ACIDZhejiang JOOZENA Medical Technology Co., Ltd.455ad304-86bc-0abe-e063-6294a90a5b432026-02-12WarningsExact identifier
ndc (package): 87259-001-01
ndc (product): 87259-001
ndc11 (package): 87259000101
spl id: 4aadaa12-6087-45e0-e063-6394a90a3af1
spl set id: 455ad304-86bc-0abe-e063-6294a90a5b43

Reported adverse events (FAERS/openFDA)#

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