Label: HAPPY NUTS JOCK ITCH POWDER- miconazole nitrate powder

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

Drug Label Information

Updated February 13, 2026

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  • Active Ingredient

    Miconazole Nitrate 2%

    Purpose

    Antifungal

  • INDICATIONS & USAGE

    for the cure of most jock itch (tinea cruris). Relieves itching, burning, cracking, scaling and discomfort 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 dyes.

    Stop use and ask a doctor if

    • irritation occurs
    • there is no improvement within 2 weeks

    Keep out of reach of children.

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

  • Directions

    • Clean affected area thoroughly.
    • Apply a thin layer of the product over the affected area twice daily (morning and night) or as directed by a doctor
    • Supervise children when using this product
    • Use daily for 2 weeks
    • If condition persists longer, consult a doctor
    • This product is not effective on the scalp or nails
  • Inactive ingredients

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

  • PRINCIPAL DISPLAY PANEL

    Happy Nuts Jock Itch Powder

    Happy Nuts Drug Facts Panel

  • INGREDIENTS AND APPEARANCE
    HAPPY NUTS JOCK ITCH POWDER 
    miconazole nitrate powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87151-111
    Route of AdministrationCUTANEOUS
    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
    STARCH, CORN (UNII: O8232NY3SJ)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    STARCH, RICE (UNII: 4DGK8B7I3S)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87151-111-0171 g in 1 BOTTLE; Type 0: Not a Combination Product11/03/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00511/03/2025
    Labeler - Suit Up Brands LLC (110713330)
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