REMEDY ANTIFUNGAL (MICONAZOLE NITRATE) POWDER [MEDLINE INDUSTRIES, INC.]

REMEDY ANTIFUNGAL (MICONAZOLE NITRATE) POWDER [MEDLINE INDUSTRIES, INC.]
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NDC 53329-169-79
Set ID 021b4a31-d7f6-4921-b4b1-cbe832eecd93
Category HUMAN OTC DRUG LABEL
Packager Medline Industries, LP
Generic Name
Product Class Azole Antifungal
Product Number
Application Number PART333C
  • Active ingredient

    Miconazole Nitrate 2%

  • Purpose

    Antifungal

  • Uses

    • For the treatment of most athlete's foot (tinea pedis), jock itch (tinea cruris), ringworm (tinea corporis)
    • For the treatment of superficial skin infections caused by yeast (candida albicans)
    • Relieves itching, scaling, cracking, burning, redness, soreness, irritation, discomfort 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
    • avoid contact with eyes
    • for athlete's foot and ringworm- if irritation occurs, or if there is no improvement within 4 weeks, discontinue use and consult a doctor
    • for jock itch - if irritation occurs or if there is no improvement within 2 weeks, discontinue use and consult a doctor

    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 layer of power over affected area twice a day (morning and night) or as directed by a doctor
    • Supervise children in the use of this product
    • For athlete's foot, pay special attention between spaces in toes; wear well fitting, ventilated shoes, and change shoes and socks at least twice 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 nails.
  • Other Information

    • Protect from freezing. Avoid excessive heat.
  • Inactive ingredients

    Aphanizomenon Flos-Aquae (Algae) Extract, Camellia Sinensis (Green Tea) Leaf

    Extract, Caprylic/Capric Triglycerides, 7-Dehydrocholesterol, Dipotassium Glycyrrhizate, Ethylene Brassylate, Eugenia Caryophyllus (Clove) Flower Extract, Glycerin, Hydrolyzed Soy Protein, Isopropyl Myristate, Methyldihydrojasmonate, Phospholipids, Silica, Sodium Benzoate, Tapioca Starch, Tocopheryl (Vitamin E) Acetate, Vanilla Plantifolia Fruit Extract, Water, Yeast Ferment Extract, Zea Mays (Corn) Oil, Zea Mays (Corn) Starch

  • Principal Display Panel

    Label 169

  • INGREDIENTS AND APPEARANCE
    REMEDY ANTIFUNGAL 
    miconazole nitrate powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-169
    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
    APHANIZOMENON FLOS-AQUAE (UNII: 49VG1X560X)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CAPRYLIC/CAPRIC/LINOLEIC TRIGLYCERIDE (UNII: U73D397055)  
    7-DEHYDROCHOLESTEROL (UNII: BK1IU07GKF)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)  
    CLOVE (UNII: K48IKT5321)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SOY PROTEIN (UNII: R44IWB3RN5)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    STARCH, TAPIOCA (UNII: 24SC3U704I)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VANILLA (UNII: Q74T35078H)  
    WATER (UNII: 059QF0KO0R)  
    YEAST (UNII: 3NY3SM6B8U)  
    CORN OIL (UNII: 8470G57WFM)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53329-169-7985 g in 1 BOTTLE; Type 0: Not a Combination Product11/19/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333C11/19/2012
    Labeler - Medline Industries, LP (025460908)