FUNGAZOL ATHLETE FOOT- miconazole nitrate cream

Fungazol Athlete Foot by

Drug Labeling and Warnings

Fungazol Athlete Foot by is a Otc medication manufactured, distributed, or labeled by Rida LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Miconazole Nitrate USP, 2%

Purpose

Antifungal

Uses

• cures most athlete’s foot (tinea pedis)
• cures most jock itch (tinea cruris) and ringworm (tinea corporis)
• relieves itching, burning, cracking and scaling which accompany theses conditions

Warnings

For external use only

Do not use

• on nails or scalp
• in or near the mouth or eyes
• for vaginal yeast infections

When using this product do not get into eyes. If eye contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if too much irritation occurs or gets worse.

Keep out of the reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Directions

Adults and children 12 years and over:

• wash affected area with soap and water and dry completely before applying
• for athlet's foo twear well-fitting, ventilated shoes. Change shoes and socks at least once daily.
• between the tose only:apply twice a day (morning and night) for 1 weekor as directed by doctor
• on the bottom or sides of the foot: apply twice a day (morning and night) for 2 weeksor as directed by doctor
• for jock itch and ringworm: apply once a day (morning ornight) for 1 weekor as directed by a doctor
• wash hands after each use
• Children under 12 years: ask a doctor

Other Information 

• do not use if seal on the tube is broken or is not visible. 
• store at controlled room temperature 20-25°C (68-77°F)

Inactive ingredients

Organic tea tree oil, benzoic acid, cetyl alcohol, isopropyl myristate, polysorbate 60, olive oil, potassium hydroxide, propylene glycol, water, stearyl alcohol

Questions or comments?

(888) 885-6137

Product label

INGREDIENTS AND APPEARANCE

FUNGAZOL ATHLETE FOOT 
miconazole nitrate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83004-025
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 mL

Inactive Ingredients
Ingredient Name	Strength
TEA TREE OIL (UNII: VIF565UC2G)
BENZOIC ACID (UNII: 8SKN0B0MIM)
CETYL ALCOHOL (UNII: 936JST6JCN)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
POLYSORBATE 60 (UNII: CAL22UVI4M)
OLIVE OIL (UNII: 6UYK2W1W1E)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83004-025-01	1 in 1 CARTON	05/23/2025
1		120 mL in 1 BOTTLE; 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	05/23/2025

Labeler - Rida LLC (004425803)