Label: ANTIFUNGAL RINGWORM TREATMENT- miconazole nitrate spray
- NDC Code(s): 83004-030-01
- Packager: Rida LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 15, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Uses
-
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.
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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
- Inactive ingredients
- Product label
-
INGREDIENTS AND APPEARANCE
ANTIFUNGAL RINGWORM TREATMENT
miconazole nitrate sprayProduct 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)

