Label: TOTAL MERCURY- mercurius vivus liquid

  • NDC Code(s): 61657-0961-1
  • Packager: White Manufacturing Inc. DBA Micro-West
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated January 21, 2021

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

View All Sections
  • ACTIVE INGREDIENTS

    MERCURIUS VIVUS [HPUS]  12X,30X,200C,1M

    Contains equal volumes of each ingredient.

  • PURPOSE

    FOR THE TEMPORARY RELIEF OF DIZZINESS, DISCOURAGED, DEPRESSION, PAINFUL DRYNESS OF THROAT

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS

    INDICATIONS :FOR THE TEMPORARY RELIEF OF DIZZINESS,FEELING  DISCOURAGED, DEPRESSION, PAINFUL DRYNESS OF THROAT

  • WARNING

    WARNING:STOP USE AND CALL A DOCTOR IF SYMPTOMS PERSIST OR WORSEN. IF PREGNANT ORBREAST-FEEDING CONSULT A HEALTHCARE PROFESSIONAL BEFORE USE.CONTAINS ALCOHOL, IN CASE OF ACCIDENTAL OVERDOSE, CONSULT A POISON CONTROL CENTER IMMEDIATELY

  • DIRECTIONS

    DIRECTIONS: ORALLY 6 DROPS ORALLY, 4 TIMES A DAY.FOR AGES 2 TO ADULT

  • INACTIVE INGREDIENT

     ALCOHOL (20% V/V,PURIFIED WATER)

  • MANUFACTURE

    MANUFACTURED FOR MICRO-WEST

    DOUGLAS, WY 82633

    1-307-358-5066

  • label

    NDC 61657-0961-1

    MICRO-WEST

    Homeopathic

    4 Tier Multi-Potency

    TOTAL MERCURY

    Product #: 0961

    1.0 fl oz bottle label

    1.0 fl oz (29.6 mL)

    Ethanol 20%

  • INGREDIENTS AND APPEARANCE
    TOTAL MERCURY 
    mercurius vivus liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61657-0961
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MERCURY (UNII: FXS1BY2PGL) (MERCURY - UNII:FXS1BY2PGL) MERCURY12 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61657-0961-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/01/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/01/2011
    Labeler - White Manufacturing Inc. DBA Micro-West (082307831)
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!