85248-146update

Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD
Effective date
2026-06-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-06-16 05:10:11

Label at a glance#

ProductEVERFERE ANTIFUNGAL
Active ingredientZINC UNDECYLENATE, UNDECYLENIC ACID
Label structure13 sections

Dosage and administration

1.Do a patch test, then clean and thoroughly dry the affected area. 2.Apply a thin layer of the product to the affected area twice daily (morning and evening). 3.If symptoms persist or worsen, consult a health care professional.

Storage and handling

■ Do not use if seal on product opening is broken or missing. ■ Store at room temperature 15°-30°C (59°-86°F). ■ Read all label directions. Keep carton, it contains important information.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Undecylenic Acid 10% (w/w) Zinc Undecylenate 12%(w/w)

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

■Proven antifungal treatment
■Relieves itching, burning, cracking, and scaling associated with:Athlete's Foot, Jock Itch, Ringworm.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

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

When Using

OTC - WHEN USING SECTION

■When using this product, avoid contact with the eyes.

Stop Use

OTC - STOP USE SECTION

■Irritation occurs. There is no improvement within 4 weeks (for athlete's foot and ringworm) or within 2 weeks (for jock itch).

Ask Doctor

OTC - ASK DOCTOR SECTION

■Irritation occurs.
There is no improvement within 4 weeks (for athlete's foot and ringworm) or within 2 weeks (for jock itch).

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■If swallowed, get medical help or contact a Poison control center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Do a patch test, then clean and thoroughly dry the affected area.
2.Apply a thin layer of the product to the affected area twice daily (morning and evening).
3.If symptoms persist or worsen, consult a health care professional.

Other information

STORAGE AND HANDLING SECTION

■ Do not use if seal on product opening is broken or missing.
■ Store at room temperature 15°-30°C (59°-86°F).
■ Read all label directions. Keep carton, it contains important information.


Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin, Aloe Barbadensis (Aloe Vera) Leaf Water, Butylene Glycol, Propylene Glycol, Cetearyl Alcohol, Glyceryl Monostearate, Chamomilla Recutita (Matricaria) Flower Water, Caprylic/Capric Triglyceride, Butyrospermum Parkii (Shea) Butter, Dimethicone, Colloidal Oatmeal, Centella Asiatica Extract, Glyceryl Stearate, Camellia Japonica Seed Oil, Ceramide NP, Potassium Sorbate, Tocopherol (Vitamin E), Portulaca Oleracea Extract, Sodium Hyaluronate.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1010

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85248-14685248-146-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-02-27full-release2026-06-01 01:47:46

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
EVERFERE ANTIFUNGALUNDECYLENIC ACID 10% ZINC UNDECYLENATE 12% ANTIFUNGALJiangxi Yudexi Pharmaceutical Co., LTD4bc99af7-ea08-8543-e063-6294a90a44cd2026-06-12WarningsExact identifier
ndc (package): 85248-146-01
ndc (product): 85248-146
ndc11 (package): 85248014601
spl id: 541946a0-6881-cfa6-e063-6394a90a3a9c
spl set id: 4bc99af7-ea08-8543-e063-6294a90a44cd

Reported adverse events (FAERS/openFDA)#

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