Label: ANTIFUNGAL POWDER- miconazole nitrate powder

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

Drug Label Information

Updated June 8, 2026

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Active Ingredient                     

    Miconazol Nitrate 2%                         

  • Purpose

    Antifungal

  • Uses

    • Proven clinically effective in the treatment of most: • athlete's foot • jock itch • ringworm • Relieves itching, scaling, cracking, burning, redness, soreness, irrita-tion, and discomforts associated with all three treatments. Also relieves chaffing associated with jock itch.

  • Warnings

    For external use only.

  • Do Not Use

    Do not use on children under 2 years of age unless directed by a doctor

  • When using this product

    Avoid contact with eyes

  • Stop use and ask a doctor if

    ■ irritation occurs

    ■ there is no improvement I within 4 weeks (for athlete's foot or ringworm) or 2 weeks (for jock itch)

  • Keep Out Of Reach Of Children

    Keep Out Of Reach Of Children

    Do not let the powder get into your eyes. This product contains talc. Do not breathe in the powder as this may cause irritation of the airways. This is especially important for children and infants. If swallowed, contact a poison control center immediately.

  • Directions

    ■ clean affected area and dry thoroughly

    ■ apply thin layer of powder to affected area twice daily (morning and night) or as direct-ed by a doctor

    ■ supervise children in the use of this product

    ■ for athlete's foot pay special attention to space between the toes; wear well-fitting, ventilated shoes and change shoes and socks at least once daily

    • for athlete's foot and ringworm, use daily for 4 weeks; for jock itch use daily for 2 weeks

    ■ if condition persists longer, consult a doctor

    •this product is not effective on the scalp or nail

  • Other information

    Store at room temperature

  • Inactive ingredients

    Colloidal silicon dioxide, Corn Starch, Dipotassium Glycyrhizinate, Sodium Benzoate

  • Questions

    Call 1-833-605-84-74 9am-5 pm EST M-F

  • Principal Display panel

    label

  • INGREDIENTS AND APPEARANCE
    ANTIFUNGAL POWDER 
    miconazole nitrate powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87236-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87236-012-0385 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00512/01/2025
    Labeler - Aldermed Inc. (144887712)
    Registrant - Aldermed Inc. (144887712)