Label: WARRIOR ANTIFUNGAL FOOT- miconazole nitrate 2% powder

  • NDC Code(s): 72839-961-02
  • Packager: Derma Care Research Labs, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 20, 2024

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  • ACTIVE INGREDIENT

    Miconazole Nitrate 2%

  • PURPOSE

    Antifungal

  • INDICATIONS & USAGE

    For the cure of athlete's foot and jock itch. Relieves itching 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 or for diaper rash. When using thisproduct avoid contact with the eyes. Stop use and ask a doctor if irritation occurs or if there is no improvement within 4 weeks.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Cleanse the affected area and dry thoroughly. Apply a thin layer of the product over the affected area twice daily or as directed by a doctor or healthcare professional. 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. Use daily for 4 weeks.

    If the condition persists, consult a doctor.

    This product is not effective on the scalp or nails.

  • INACTIVE INGREDIENT

    Corn Starch, Fragrance, Potassium Sorbate, Rice Starch, Sodium Benzoate.

  • PRINCIPAL DISPLAY PANEL

    LabelLabel

  • INGREDIENTS AND APPEARANCE
    WARRIOR ANTIFUNGAL FOOT 
    miconazole nitrate 2% powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72839-961
    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
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    STARCH, RICE (UNII: 4DGK8B7I3S)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72839-961-0271 g in 1 BOTTLE; Type 0: Not a Combination Product02/02/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00502/02/2021
    Labeler - Derma Care Research Labs, LLC (116817470)
    Registrant - Derma Care Research Labs, LLC (116817470)
    Establishment
    NameAddressID/FEIBusiness Operations
    Derma Care Research Labs, LLC116817470manufacture(72839-961)
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