Label: DR. ZHENG S ACTERIOSTATIC GEL- bacteriostatic gel gel

  • 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 11, 2020

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  • DOSAGE & ADMINISTRATION

    Please store in a cool and dry place.

  • INACTIVE INGREDIENT

    Betula platyphylla extract

  • INDICATIONS & USAGE

    Hand sanitization:take this product in the palm of your hand,and coat each part evenly with your hands for 1 minute.Disinfection of operation hand: clean and dry the hands,forearms and 1/ 3 of the lower part of the upper arm according to the specification, take 5-10g of this product and evenly spreadit on the hands, forearms and the lower part of the upper arm,rub it until it is dry, function for 3 minutes, and then wear sterilegloves.
    Hand disinfection in daily work: take 3G of this product andknead it for 1 minute.

  • ACTIVE INGREDIENT

    Chlorhexidine acetate

  • KEEP OUT OF REACH OF CHILDREN

    keep out of children

  • PURPOSE

    Disinfection
    Sterilization
    No Rinseing

  • WARNINGS

    1.This product is a disinfectant for external use and should not be taken orally.
    2.Keep out of reach of children.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DR. ZHENG S ACTERIOSTATIC GEL 
    bacteriostatic gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42091-002
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE ACETATE0.55 g  in 500 g
    Inactive Ingredients
    Ingredient NameStrength
    BETULA PLATYPHYLLA BARK (UNII: ZF70YKN0YO)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42091-002-01500 g in 1 BOTTLE; Type 0: Not a Combination Product04/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/11/2020
    Labeler - Guangzhou Yuxiao Biological Products Co., Ltd. (420915194)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yuxiao Biological Products Co., Ltd.420915194manufacture(42091-002)