ANTIFUNGAL RINGWORM TREATMENT- miconazole nitrate spray

Antifungal Ringworm Treatment by

Drug Labeling and Warnings

Antifungal Ringworm Treatment by is a Otc medication manufactured, distributed, or labeled by Rida LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Miconazole Nitrate 2%

Purpose

Anti-fungal

Uses

• effectively treats most of  cases of ringworm (tinea corporis) and related fungal infections.
• helps relieve itching, redness, flaking, and irritation commonly associated with ringworm and similar skin conditions.

Directions

Adults and children 12 years and over

• Wash the affected skin with soap and water and dry completely before applying.
• for ringworm: apply a thin layer to the affected skin once daily (morning  or night) for 1 week, or as directed by a doctor
• severe or persistent cases: use twice daily (morning  and evening) for up to 2 weeks, or as directed by a doctor
• allow the product to fully dry on the skin before dressing
• wash hands after each use children under 12 years: ask a doctor.

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

Other Information

• do not use if seal on box is brken 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, Oxygenated olive oil, Potassium hydroxide, Propylene glycol, Purified water, Stearyl alcohol, Mel (Manuka Honey) Extract.

Product label

INGREDIENTS AND APPEARANCE

ANTIFUNGAL RINGWORM TREATMENT 
miconazole nitrate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83004-030
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
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
ETHYLPARABEN (UNII: 14255EXE39)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83004-030-01	1 in 1 CARTON	01/14/2026
1		120 mL in 1 TUBE; 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	01/14/2026

Labeler - Rida LLC (004425803)