FUNGIFREE Jock Itch & Psoriasis Treatment Cream

FUNGIFREE Jock Itch Psoriasis Treatment Cream by

Drug Labeling and Warnings

FUNGIFREE Jock Itch Psoriasis Treatment Cream by is a Otc medication manufactured, distributed, or labeled by YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FUNGIFREE JOCK ITCH PSORIASIS TREATMENT CREAM- miconazole nitrate cream 
YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD

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FUNGIFREE Jock Itch & Psoriasis Treatment Cream

Drug Facts

Active ingredients

Miconazole Nitrate 2%

Purpose
Anti-Fungal

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

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

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

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

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

WARNINGS
- For external use only

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.

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

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

FUNGIFREE JOCK ITCH PSORIASIS TREATMENT CREAM 
miconazole nitrate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83364-014(NDC: 84010-009)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
CHLORHEXIDINE DIACETATE (UNII: 5908ZUF22Y)
STEARIC ACID (UNII: 4ELV7Z65AP)
BASSIA SCOPARIA FRUIT (UNII: 04W97Z676Y)
SILVER (UNII: 3M4G523W1G)
ZINC OXIDE (UNII: SOI2LOH54Z)
WHITE PETROLATUM (UNII: B6E5W8RQJ4)
CAMELLIA OIL (UNII: T1PE06G0VE)
ALLANTOIN (UNII: 344S277G0Z)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
LAUROCAPRAM (UNII: 1F3X9DRV9X)
GLYCERIN (UNII: PDC6A3C0OX)
MENTHOL (UNII: L7T10EIP3A)
LONICERA CONFUSA FLOWER (UNII: 3JV904IJ0V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83364-014-01	1 in 1 BOX	12/09/2024	05/31/2025
1		60 g in 1 CANISTER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	12/09/2024	05/31/2025

Labeler - YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD (725220463)

Revised: 6/2025

Document Id: 3843ea65-260a-c0a3-e063-6394a90a47cf

34390-5

Set id: 28a00fbf-7335-85dc-e063-6294a90ab620

Version: 2

Effective Time: 20250623

 

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