Label: MICONAZOLE- miconazole nitrate cream

  • NDC Code(s): 68016-291-01
  • Packager: Chain Drug Consortium, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 20, 2018

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  • Drug Facts

  • Active ingredient

    Miconazole nitrate, USP 2%

  • Purpose

    Antifungal

  • Uses

    • proven clinically effective in the treatment of most athlete's foot, jock itch, and ringworm
    • for effective relief of itching, scaling, cracking, burning, and discomfort
  • 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 use and ask a doctor if

    • irritation occurs
    • there is no improvement within 4 weeks (for athlete's foot and ringworm) or within 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

    • wash 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, 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 lasts longer, contact a doctor
    • this product is not effective on the scalp or nails
  • Other information

    • store at controlled room temperature 59°-86°F (15°-30°C).
    • before using any medication, read all label directions. Keep carton, it contains important information.
  • Inactive ingredients

    benzoic acid, butylated hydroxyanisole, mineral oil, oleoyl polyoxylglycerides, pegoxol 7 stearate, purified water

  • Questions?

    1-800-432-8534 between 9 am and 4 pm EST, Monday-Friday.

  • Principal Display Panel

    Premier Value®

    COMPARE TO THE ACTIVE INGREDIENT IN MICATIN® ANTIFUNGAL CREAM*

    Miconazole Nitrate Cream, USP 2%
    ANTIFUNGAL CREAM

    Cures Most Athlete’s Foot, Jock Itch & Ringworm. 

    Soothes Itching, Scaling, Cracking, and Burning 

    NET WT 1 OZ (28g)

    1 oz carton
  • INGREDIENTS AND APPEARANCE
    MICONAZOLE 
    miconazole nitrate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-291
    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
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PEGOXOL 7 STEARATE (UNII: 3EW5AXE5X5)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68016-291-011 in 1 CARTON05/15/2009
    128 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart333C05/15/2009
    Labeler - Chain Drug Consortium, LLC (101668460)
    Registrant - Teva Pharmaceuticals USA, Inc. (001627975)