ATHLETES FOOT- miconazole nitrate cream

Athletes Foot by

Drug Labeling and Warnings

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

When using this productdo not get into eyes. If eye contact occurs, rinse thoroughly with water.
Stop use and ask a doctor iftoo 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 footwear 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 weeks or 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 box 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

Product label

INGREDIENTS AND APPEARANCE

ATHLETES FOOT 
miconazole nitrate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83004-014
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: 83004-014-01	1 in 1 CARTON	02/27/2025
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	02/27/2025

Labeler - Rida LLC (004425803)