Label: ZEASORB JOCK ITCH- miconazole nitrate powder

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

Drug Label Information

Updated November 10, 2023

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  • Active ingredient

    Miconazole nitrate 2%

  • Purpose

    Antifungal

  • Use

    • Proven clinically effective in the treament of most jock itch
  • Warnings

    For external use only.

    Avoid contact with the eyes.

    Do not use

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

    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

    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. Use daily for 2 weeks. If condition persists longer, consult a doctor. This product is not effective on the scalp or nails.

  • Other information

    • store at 20 o - 25 oC (68 o - 77 oF) [see USP Controlled Room Temperature]. Product settles during shipment. Package contains full net weight.
  • Inactive ingredients

    Aloe Barbadensis Leaf Juice Powder, Bentonite, Fragrance, Potassium Sorbate, Sodium Benzoate, Tapioca Starch, Tricalcium Phosphate, Water, Zea Mays (Corn) Starch

  • Questions?

    call 1-833-279-6522

  • Principal Display

    New & Improved

    Zeasorb®AF

    Antifungal Powder

    with 2% Miconazole Nitrate

    Cures Most Jock Itch

    Relieves Itching, Burning, Scaling

    Patented Odor Control Technology

    Attacks and Absorbs Moisture

    Talc-Free, Paraben-Free, Aluminum-Free

    Dermatologist Recommended

    Net wt. 2.5 oz (71g)

    P12322.00

    Zeasorb JI

  • INGREDIENTS AND APPEARANCE
    ZEASORB JOCK ITCH 
    miconazole nitrate powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-8001
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    STARCH, TAPIOCA (UNII: 24SC3U704I)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    WATER (UNII: 059QF0KO0R)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    BENTONITE (UNII: A3N5ZCN45C)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0316-8001-0271 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/19/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00510/19/2023
    Labeler - Crown Laboratories (079035945)
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