Label: HOQU NAIL FUNGUS LIQUID- nail fungus liquid liquid

  • NDC Code(s): 84095-001-01
  • Packager: Shenzhen Suai Electronic Science & Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 18, 2024

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  • Active Ingredient

    chlorhexidine acetate 0.35%

  • Purpose

    bacteriostatic, sterilizing.

  • Use

    Use for fungal nail infections.

  • Warnings

    For external use only

  • Do not use

    It is prohibited for those who are allergic to this product and pregnant women, and should be used with caution on open wounds.

  • When Using

    Do not put in eyes,If it accidentally gets into your eyes, rinse with water or seek medical advice.If irritation or rash occurs, discontinue use and ask a doctor. If swallowed, get medical help or contact a Poison Control Center immediately

  • Stop Use

    Stop use and ask a doctor if irritation or rash occurs.

  • Ask Doctor

    Do not put in eyes,lfit accidentally gets into your eyes, rinse with water or seek medical advice.lfirritation or rash occurs, discontinue use and ask a doctor. if swallowed, get medical help orcontact a Poison Control Centerimmediatel

  • Keep Oot Of Reach Of Children

    Please keep this product out of reach of children.

  • Directions

    Apply this product to the desired nail area, 1-2 times a day. Keep using it. Avoid light, airtight, and store in a cool and dry place.

  • Inactive ingredients

    borneol,Cnidium monnieri (L.) Cuss,CORTEX DICTAMNI,Impatiens balsamina L,Pseudolarix kamepferi Gord, Sophora flavescens Alt, water.

  • PRINCIPAL DISPLAY PANEL

    123

  • INGREDIENTS AND APPEARANCE
    HOQU NAIL FUNGUS LIQUID 
    nail fungus liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84095-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE ACETATE0.35 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    IMPATIENS IRVINGII WHOLE (UNII: 2VRX978X4A)  
    WATER (UNII: 059QF0KO0R)  
    DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)  
    BORNEOL (UNII: M89NIB437X)  
    CNIDIUM OFFICINALE WHOLE (UNII: E9V83DB6BY)  
    SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)  
    HIBISCUS SYRIACUS BARK (UNII: U6PQI719P3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84095-001-0120 mL in 1 BOTTLE; Type 0: Not a Combination Product02/18/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00502/18/2024
    Labeler - Shenzhen Suai Electronic Science & Technology Co., Ltd. (444420123)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Suai Electronic Science & Technology Co., Ltd.444420123manufacture(84095-001) , label(84095-001)
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