Label: TOTAL ANTIMONY - antimonium tartaricum liquid

  • NDC Code(s): 61657-0966-1
  • 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 April 20, 2016

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  • Active Ingredients

    antimonium tartaricum  12x,30x,200c,1m

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  • Uses

    Metallic taste, gout-like symptoms, angina, anorexia, fatigue, myopathy, hypotension,

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  • Keep Out of Reach of Children

    KEEP OUT OF REACH OF CHILDREN

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  • INDICATIONS

    INDICATIONS:  Metallic taste, gout-like symptoms, angina, anorexia, fatigue, myopathy, hypotension, "antimony spots" if exposed to vapor

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  • Ask Doctor

    If pregnant or nursing, please consult physician before using this product

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  • Directions

    Directions: Orally 6 drops, 4 times a day

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  • Inactive Ingredient

    Not more than 20% Alcohol

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  • SPL UNCLASSIFIED SECTION

    Manufactured for Micro West

    Douglas, WY 82633

    1-307-358-5066

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  • Principal Display Panel
  • INGREDIENTS AND APPEARANCE
    TOTAL ANTIMONY  
    antimonium tartaricum liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:61657-0966
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE 12 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient Name Strength
    Alcohol (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:61657-0966-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 11/04/2015
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 07/13/2011
    Labeler - White Manufacturing Inc. DBA Micro -West (082307831)
    Establishment
    Name Address ID/FEI Business Operations
    King Bio 617901350 manufacture(61657-0966) , pack(61657-0966) , label(61657-0966)
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