Label: ANTIFUNGAL POWDER- miconazole nitrate powder

  • NDC Code(s): 70000-0679-1
  • Packager: LEADER/ Cardinal Health 110, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 31, 2025

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  • Active ingredient

    Miconazole nitrate 2%

  • Purpose

    Antifungal

  • Uses

    for the cure of most athlete's foot, ringworm and chafing associated with jock itch

  • Warnings

    For external use only.

    Do not use

    on children under 2 years of age unless directed by a doctor.

    When using this product

    avoid contact with the eyes

    Stop and ask a doctor if

    irritation occurs or there is no improvement within 4 weeks for athlete's foot and ringworm, or 2 weeks for jock itch.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • clean the affected area and dry thoroughly
    • apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor
    • supervise children in the use of this product
    • for athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, & change shoes & socks at least once daily
    • for athlete's foot & ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks
    • if conditions persist longer, consult a doctor
    • this product is not effective on the scalp or nails
  • Other information

    • store between 59º - 86ºF
    • lightly shake bottle to loosen settled powder
  • Inactive ingredients

    Zea Mays (Corn) Starch, Tricalcium Phosphate, Microcrystalline Cellulose, Sodium Bicarbonate, Allantoin, Chloroxylenol, Fragrance

  • Questions?

    Call 1-866-964-0939

  • Principal Display Panel

    LEADER

    Moisture Absorbing

    Antifungal

    Powder

    Miconazole Nitrate 2%/

    Antifungal

    Cures Most Athlete's Foot

    Relieves Itching, Burning

    & Scaling

    Absorbs Moisture

    COMPARE TO

    ZEASORB AF

    active ingredient

    NET WT 2.5 OZ (71 g)

    carton

  • INGREDIENTS AND APPEARANCE
    ANTIFUNGAL POWDER 
    miconazole nitrate powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0679
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    CHLOROXYLENOL (UNII: 0F32U78V2Q)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70000-0679-171 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/16/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00508/16/2024
    Labeler - LEADER/ Cardinal Health 110, Inc. (063997360)
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