Label: TOTAL ANTIMONY  - antimony potassium tartrate liquid 

  • Label RSS
  • 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

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 09/12

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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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  • Principal Display Panel
  • SPL UNCLASSIFIED SECTION

    Manufactured for Micro West

    Douglas, WY 82633

    1-307-358-5066

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  • INGREDIENTS AND APPEARANCE
    TOTAL ANTIMONY  
    antimonium tartaricum liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:61657-0966
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ANTIMONY POTASSIUM TARTRATE (ANTIMONY CATION (3+)) ANTIMONY POTASSIUM TARTRATE 12 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient Name Strength
    Alcohol  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:61657-0966-1 30 mL in 1 BOTTLE, DROPPER
    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
    White Manufacturing Inc. DBA Micro -West 082307831 label(61657-0966), pack(61657-0966)
    Establishment
    Name Address ID/FEI Business Operations
    Washington Homeopathic Products 084929389 manufacture(61657-0966)
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