Label: HOQU NAIL FUNGUS SOLUTION- nail fungus solution liquid

  • NDC Code(s): 84095-004-01
  • Packager: Shenzhen Suai Electronic Science & Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 9, 2024

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  • Active Ingredient

    chlorhexidine acetate 0.2% v/v

  • 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,lf it accidentally gets into your eyes, rinse with water or seek medical advice.lf irritation or rash occurs, discontinue use and ask a doctor. if swallowed, get medical help or contact a Poison Control Center immediately

  • 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

    ARTEMISIA ARGYI LVL.ET VAN,ANGELICAE DAHURICAE RADIX,IMPATIENS BALSAMINA L,PHRYMA L,PSEUDOLARIX KAMEPFERI GORD,SOPHORA FLAVESCENS,STEMONASESSILIFOLIA,WATER.

  • PRINCIPAL DISPLAY PANEL

    123456

  • INGREDIENTS AND APPEARANCE
    HOQU NAIL FUNGUS SOLUTION 
    nail fungus solution liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84095-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE ACETATE0.2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ)  
    SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)  
    PSEUDOLARIX AMABILIS WHOLE (UNII: G2TMJ38TAU)  
    ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)  
    IMPATIENS BALSAMINA LEAF (UNII: LH9E1X602V)  
    PHRYMA LEPTOSTACHYA WHOLE (UNII: 6G287VJM69)  
    3-METHYL-5-HEPTANONE OXIME (UNII: XHN6C9A7U3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84095-004-0120 mL in 1 BOTTLE; 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 - Shenzhen Suai Electronic Science & Technology Co., Ltd. (444420123)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Suai Electronic Science & Technology Co., Ltd.444420123manufacture(84095-004) , label(84095-004)
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