Label: CHARMPOO ANTIFUNGAL CREAM- antifungal cream cream

  • NDC Code(s): 84010-046-01, 84010-046-02
  • Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 20, 2024

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  • Active Ingredient

    miconazole nitrate 2% w/w

  • Purpose

    Anti-fungal

  • Use

    The product with Repair and Anti-ltch function effectively relieve skin discomfort, such as itching, athlete's foot eczema, jock itch, etc

  • Warnings

    For external use only

  • Do not use

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

  • When Using

    avoid contact with the eyes.

  • Stop Use

    ·Irritation occurs

    ·There is no improvement within 4 weeks (for athlete's foot and fingworm) or within 2 weeks (for jock itch)

  • Ask Doctor

    ·Irritation occurs

    ·There is no improvement within 4 weeks (for athlete's foot and fingworm) or within 2 weeks (for jock itch)

  • Keep Oot Of Reach Of Children

    lf swallowed, get medical help or contact a Poison controlcenter(1-800-222-1222)right away.

  • Directions

    Apply suitable amount unto the affected skin 2-3 times daily and massage until absorbs.

  • Other information

    ·Do not use if seal on product opening is broken or missing

    ·Store at room temperature 15°-30°C(59°-86°F)

    ·Read all label directions. Keep carton, it contains important information.

  • Inactive ingredients

    Purifed water, Aloe, Borneol, Chlorhexidine acetate, Cnidium, Dictamnus,Euphorbia, Glycerin, Lightliquid paraffn, Medical vaseline, Natural menthol Sophora Flavescens, Stearic acid, Stemona,Triethanolamine, Vitamin E

  • Questions

    Any questions, please email to support@charmpooskincare.com

  • PRINCIPAL DISPLAY PANEL

    12

  • INGREDIENTS AND APPEARANCE
    CHARMPOO ANTIFUNGAL CREAM 
    antifungal cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84010-046
    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
    ALOE (UNII: V5VD430YW9)  
    VASICINONE (UNII: G6T5819NXM)  
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEMONA JAPONICA ROOT (UNII: FXG254HF10)  
    WATER (UNII: 059QF0KO0R)  
    BORNEOL (UNII: M89NIB437X)  
    DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)  
    CNIDIUM MONNIERI FRUIT EXTRACT (UNII: V1IA3S3CUS)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    EUPHORBIA NERIIFOLIA LEAF (UNII: IRZ1UXK5K9)  
    MENTHOL (UNII: L7T10EIP3A)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    TRIETHANOLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84010-046-0130 g in 1 TUBE; Type 0: Not a Combination Product11/20/2024
    2NDC:84010-046-02100 g in 1 BOTTLE; Type 0: Not a Combination Product11/20/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00511/20/2024
    Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangxi Hemei Pharmaceutical Co., Ltd724892056manufacture(84010-046)
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