Label: NAIL FUNGUS TREATMENT- tomumia nail fungus liquid

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

Drug Label Information

Updated June 13, 2024

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  • Active Ingredient

    Chlorhexidine acetate (3%)

  • Purpose

    for Toenails & Fingernails /Restores Fungus Damaged Nails

  • Use

    (Usage)
    Clean the affected area with soap and warm water and dry thoroughly.
    Gently file thickened part of the fungal nail with a nail file until it's flat.
    Using the brush, apply a thin layer of liquid onto the affected area.
    Repeat this process 2 times daily for
    1-2 weeks (or) until the infection is gone

  • Warnings

    For external use only

    Keep out of the reach of children.

  • Do not use

    Avoidcontact with eyes and mouth. Donot use it on the irritated skin. Notsuitable for pregnant andbreastfeeding.

  • When Using

    Using the brush, apply a thin layer of liquid onto the affected area

  • Stop Use

    lf swallowed, get medicalassistance or contact the poison control center.

  • Ask Doctor

    lf swallowed, get medicalassistance or contact the poison control center.

  • Keep Oot Of Reach Of Children

    Keep out of the reach of children.

  • Directions

    1. For thickened and hard nails, itmust be thinned before use.

    2.lf there is a slight deposit, it is thechinese medicinal material, feel
    free to use it.

    3. After healthy nails grow, takecare and do not file them. Alwayskeep the hands and feet clean,After the nails are normal, continue
    to use for 30 days.

  • Other information

    Store at room temperature
    Avoid excessive heat 37°C (99°F)

  • Inactive ingredients

    Impatiens
    Sophora flavescens
    Tougu grass
    Stemona
    Angelicadahurica dahurica
    Vitex barkWormwood leaf
    chlorhexidine
    acetate
    water

  • Questions

    1-9146081258

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    NAIL FUNGUS TREATMENT 
    tomumia nail fungus liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83299-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE ACETATE0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANGELICA DAHURICA SEED (UNII: 9M69B50875)  
    CHLORHEXIDINE (UNII: R4KO0DY52L)  
    ILEX CORNUTA WHOLE (UNII: 9WEY0RQ9HO)  
    VITEXIN (UNII: 9VP70K75OK)  
    SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)  
    IMPATIENS WALLERIANA WHOLE (UNII: 8W4759RC84)  
    ACETATE ION (UNII: 569DQM74SC)  
    STEMONA TUBEROSA WHOLE (UNII: 9373ZOT316)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83299-030-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00506/13/2024
    Labeler - Consilii LLC (118891890)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consilii LLC118891890label(83299-030) , manufacture(83299-030)