Label: AOSORW ANTIFUNGAL CREAM- miconazole nitrate 2% cream

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

Drug Label Information

Updated June 29, 2026

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  • ACTIVE INGREDIENT

    Miconazole Nitrate 2%

  • PURPOSE

    Antifungal

  • INDICATIONS & USAGE

    • For the treatment of athlete's foot (tinea pedis), jock itch (tinea cruris), ringworm (tinea corporis).
    • Relieves itching, burning, cracking, scaling, and discomfort caused by fungal infections.
  • WARNINGS

    For external use only

    before use if you have

    • a condition that covers a large area of the body
    • sensitive skin or any known allergies to the ingredients

    on children under 2 years of age except under the advice and supervision of a doctor.

    avoid contact with eyes.

    and ask a doctor if

    • irritation occurs.
    • there is no improvement within 4 weeks (for athlete's foot and ringworm) or 2 weeks (for jock itch).

    ask a health professional before use

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

  • DOSAGE & ADMINISTRATION

    • wash affected area and dry thoroughly.
    • apply 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.
    • for athlete's foot and ringworm use daily for 4 weeks, for jock itch use daily for 2 weeks.
    • if conditions persist longer, ask a doctor.
    • this product is not effective on the scalp or nails.
  • OTHER SAFETY INFORMATION

    Store at 20ºC to 25ºC (68ºF to 77ºF).
    Close the cap tightly after use.

  • INACTIVE INGREDIENT

    Sophora Flavescens Root, Glycerin, Propylene Glycol, Peppermint Oil, Sodium Acrylate, Sodium Acryloyldimethyl Taurate, Isohexadecane, Polysorbate-80, Dimethicone, Triethanolamine

  • QUESTIONS

    Contact us at service@aosorw.com

  • PRINCIPAL DISPLAY PANEL

    product image

  • INGREDIENTS AND APPEARANCE
    AOSORW ANTIFUNGAL CREAM 
    miconazole nitrate 2% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85498-011
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM ACRYLOYLDIMETHYLTAURATE (UNII: 2T9Q6EKI0G)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    SODIUM ACRYLATE (UNII: 7C98FKB43H)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    TRIETHANOLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85498-011-01120 g in 1 JAR; Type 0: Not a Combination Product04/30/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00504/30/2025
    Labeler - SpineStatus LLC (126780339)
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