Label: CHARMPOO ANTIFUNGAL CREAM- antifungal cream cream

  • NDC Code(s): 84010-009-01
  • Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 10, 2024

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  • Active Ingredient

    miconazole nitrate 2% w/w

  • Purpose

    Anti-fungal

  • Use

    The product with Repairand Anti-ltch functioneffectivelyrelieve skindiscomfort, such asitching, athlete's footeczema, jockitch, et

  • Warnings

    •For external use only.Avoid direct contactwith eyes.

    •lfirritationoccurs,discontinue use.

    • Keep out of reach ofchildren.

    •Store in acool, darkplace

  • Do not use

    •For external use only.Avoid direct contactwith

  • When Using

    1. First test a smallpatch of skin to checkfor any potentialallergicreaction.

    2. Apply topically 2-3times daily to theaffected area.

  • Stop Use

    Stop use and ask a doctor if irritation or rash occurs. There may besigns of a serious condition. Stop use if there is no improvement
    within 4 weeks.

  • Ask Doctor

    Stop use and ask a doctor if irritation or rash occurs. There may besigns of a serious condition. Stop use if there is no improvementwithin 4 weeks.

  • Keep Oot Of Reach Of Children

    Keep it away from children. Seal the bottle and place it in acool and dry place.

  • Directions

    1. First test a smallpatch of skin to checkfor any potentialallergicreaction

    2. Apply topically 2-3times daily to the affected area.

  • Other information

    Keep it away from children. Seal the bottle and place it in acool and dry place.

  • Inactive ingredients

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

  • Questions

    Email at support@charmpoo-intl.com

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    CHARMPOO ANTIFUNGAL CREAM 
    antifungal cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84010-009
    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
    STEMONA JAPONICA ROOT (UNII: FXG254HF10)  
    ALOE (UNII: V5VD430YW9)  
    WATER (UNII: 059QF0KO0R)  
    EUPHORBIA NERIIFOLIA LEAF (UNII: IRZ1UXK5K9)  
    DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)  
    MENTHOL (UNII: L7T10EIP3A)  
    VASICINONE (UNII: G6T5819NXM)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)  
    BORNEOL (UNII: M89NIB437X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84010-009-01100 g in 1 CANISTER; Type 0: Not a Combination Product04/09/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00504/09/2024
    Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangxi Hemei Pharmaceutical Co., Ltd724892056label(84010-009) , manufacture(84010-009)
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