FUNGIFREE Jock Itch Psoriasis Treatment Cream

Manufacturer
YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD
Effective date
2025-09-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:26

Label at a glance#

ProductFUNGIFREE Jock Itch Psoriasis Treatment Cream
Active ingredientMICONAZOLE NITRATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Facts  Drug Facts(1)Drug Facts(1)

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Miconazole Nitrate 2%

OTC - PURPOSE SECTION

Purpose
Anti-Fungal

OTC - DO NOT USE SECTION

- Do not use it on children under 12 years of age unless directed by a doctor.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. In case of contact, rinse thoroughly with water.

OTC - ASK DOCTOR SECTION

Stop and ask a doctor if irritation occurs or there is no improvement within 4 weeks

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away

INDICATIONS & USAGE SECTION

USES
- Treats most jock itch (tinea cruris), psoriasis, ringworm, athlete's foot
- Relieves the itching, irritation, redness, scaling, and discomfort accompanying these conditions

WARNINGS SECTION

WARNINGS
- For external use only

DOSAGE & ADMINISTRATION SECTION

Directions
Clean and thoroughly dry the affected area.
Apply a thin layer of cream over affected areas twice daily (morning and night).or as directed by a doctor.
This product is not effective on the scalp or nails.

STORAGE AND HANDLING SECTION

Other information
Store at room temperature 15°-30°C(59°-86°F), away from excess heat and direct sun

INACTIVE INGREDIENT SECTION

Inactive ingredients
Chlorhexidine Diacetate, Cetyl-Stearyl Alcohol, White Vaseline, Glycerin, Stearic Acid, Azone, Menthol, Allantoin, Teaoil, Dictamni Cortex, Fructus Kochiae, Nano-silver, Honeysuckle, Aloe Vera Extract, Zinc Oxide, Glyceryl Stearate

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83364-02183364-021-01
84010-009

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
51a38d71-17cc-839a-e063-6394a90a25ed3dce4b4f-d521-41ea-acfe-e3617d974fe22026-05-12WarningsExact identifier
spl set id: 3dce4b4f-d521-41ea-acfe-e3617d974fe2

Reported adverse events (FAERS/openFDA)#

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