Label: MICONAZOLE NITRATE- jock itch spray aerosol, spray

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

Drug Label Information

Updated January 31, 2024

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  • Active ingredient

    Miconazole nitrate 2%

  • Purpose

    Antifungal

  • Uses

    • cures most jock itch (tinea cruris)
    • relieves itching, burning and chafing associated with jock itch
  • Warnings

    For external use only.

    Flammable:

    Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120°F. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

    When using this product

    • do not get into eyes or mouth
    • use only as directed

    Stop use and ask a doctor if

    • irritiation occurs
    • no improvement within 2 weeks

    Do not use

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

    Keep out of reach of children.

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

  • Directions

    • wash affected area and dry thoroughly
    • shake can well and spray a thin layer over affected area twice daily

    (morning and night) or as directed by a doctor

    • supervise children in the use of this product
    • use daily for two weeks; if condition persists, consult a doctor
    • this product is not effective on the scalp or nails
    • if nozzle clogs, clean with a pin
  • Other information

    store between 20° and 30°C (68° and 86°F)

  • Inactive ingredients

    disteardimonium hectorite, isobutane, kaolin, SD alcohol 40-B, zea mays (corn) starch

  • Questions?

    800-632-6900

  • Principal Display Panel

    Kroger

    Antifungal

    Jock Itch

    Powder

    Spray

    Miconazole Nitrate 2%

    Cures Most Jock Itch

    Relieves Itching,

    Chafing & Burning

    Talc-Free

    NET WT 4.6 OZ(130g)

    AF Jock Itch

  • INGREDIENTS AND APPEARANCE
    MICONAZOLE NITRATE 
    jock itch spray aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-089
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE1.3 g  in 130 g
    Inactive Ingredients
    Ingredient NameStrength
    KAOLIN (UNII: 24H4NWX5CO)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    ISOBUTANE (UNII: BXR49TP611)  
    ALCOHOL (UNII: 3K9958V90M)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30142-089-46130 g in 1 CAN; Type 0: Not a Combination Product04/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00504/01/2018
    Labeler - Kroger Co. (006999528)
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