Label: DUOAN CHLORINE CONTAINING DISINFECTANT- disinfectant liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated April 15, 2020

If you are a consumer or patient please visit this version.

  • DOSAGE & ADMINISTRATION

    Please do not put it in a dry place.

  • INACTIVE INGREDIENT

    Glacial acetic acid
    pure water

  • INDICATIONS & USAGE

    1.If it is rubbing the skin ,it can use Spraying.

    2.If it is rubbing theAir, Object Surface,Skin (Injection Site and Surgical Field),Traumatic Wound,Infected Wounds.Surgical Incision,Mucous Membrane(Conducted by Health and Medical Institutions Only),it can use Spraying and Smearing.

  • ACTIVE INGREDIENT

    Sodium hypochlorite

  • KEEP OUT OF REACH OF CHILDREN

    keep out of children

  • PURPOSE

    Disinfection
    Sterilization

  • WARNINGS

    1. The product is acidic, so please avoid sharing with alkaline substances.
    2. Use the product first when sharing with other external products.
    3. The bottle cap should be tight closed after use, and the use period is 2 weeks after opening, so please use it within the validity period.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DUOAN CHLORINE CONTAINING DISINFECTANT 
    disinfectant liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55117-001
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L) (SOPHORA FLAVESCENS WHOLE - UNII:X8KX602M5L) SOPHORA FLAVESCENS WHOLE1.5 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ACETIC ACID (UNII: Q40Q9N063P)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55117-001-011 L in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/15/2020
    Labeler - Shanxi Zhongyuyuan Biotechnology Co., Lt D. (551175650)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shanxi Zhongyuyuan Biotechnology Co., Lt D.551175650manufacture(55117-001)