Label: DR. ZHENG BACTERIOSTATIC SOLUTION- bacteriostatic solution 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 11, 2020

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

View All Sections
  • DOSAGE & ADMINISTRATION

    Please store in a cool and dry place.

  • INACTIVE INGREDIENT

    Phellodendron extract

    Betula platyphylla extract

  • INDICATIONS & USAGE

    before use, please shake it well, press the pump head at an angle of 45 : spray it directly on the hand skin, and then gently wipe it evenly. It is recommended to spray it about 20cm away from the skin, with better atomization effect. When swimming or continuing outdoor activities, please repeat spraying in time.

  • ACTIVE INGREDIENT

    CETRIMONIUM BROMIDE

  • KEEP OUT OF REACH OF CHILDREN

    keep out of children

  • PURPOSE

    Disinfection
    Sterilization

  • 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 BACTERIOSTATIC SOLUTION 
    bacteriostatic solution liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42091-001
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETRIMONIUM BROMIDE (UNII: L64N7M9BWR) (CETRIMONIUM - UNII:Z7FF1XKL7A) CETRIMONIUM BROMIDE0.125 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BETULA PLATYPHYLLA BARK (UNII: ZF70YKN0YO)  
    PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42091-001-01100 mL 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(42091-001)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!