everfere antifungal cream

Manufacturer
Guangdong Renhe Guozhuang Biotechnology Co., Ltd.
Effective date
2025-09-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:30

Label at a glance#

Producteverfere antifungal cream
Active ingredientUNDECYLENIC ACID, ZINC UNDECYLENATE
Label structure12 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(s)

OTC - ACTIVE INGREDIENT SECTION

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

Purpose

OTC - PURPOSE SECTION

Anti-fungal

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.

OTC - WHEN USING SECTION

When using this product, avoid contact with the eyes.

OTC - STOP USE SECTION

Stop use and ask a doctor if: mlrritation occurS,
There is no improvement within 4 weeks (for athlete's foot and
ringworm) or within 2 weeks (for jock itch).

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. mif swallowed, get medical help or
contact a Poison control center(1-800-22-1222) 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 Tigyceride, Butyrospermum Parki (Shea) Butter
Dimethicone, Cllidal 0atmeal, Centella Asiatica Extract, GlyceryI Stearate, Camellia Japonica Seed 0il, Ceramide NP, Potassium
Sorbate, Tocopherol (Vitamin E), Portulaca 0leracea Extract, Sodium Hyaluronate.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85435-00485435-004-01

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

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
48560166-18e0-bf27-e063-6394a90a1a0a3f5a9860-fbae-f8e2-e063-6394a90a3a7b2026-01-14WarningsExact identifier
spl set id: 3f5a9860-fbae-f8e2-e063-6394a90a3a7b

Reported adverse events (FAERS/openFDA)#

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