Label: ANTIFUNGAL RINGWORM TREATMENT- miconazole nitrate spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 15, 2026

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  • 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

    image description

  • INGREDIENTS AND APPEARANCE
    ANTIFUNGAL RINGWORM TREATMENT 
    miconazole nitrate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83004-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83004-030-011 in 1 CARTON01/14/2026
    1120 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00501/14/2026
    Labeler - Rida LLC (004425803)