Label: STOP 20-PM- antimony potassium tartrate, aconitum napellus, phosphorus, potassium carbonate, mercurius solubilis, bryonia alba, paris quadrifolia liquid

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

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 August 29, 2022

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

View All Sections
  • PURPOSE

    Helps to reduce the incidence and severity of EIPH (bleeding) in performance horses.

  • DIRECTIONS

    Orally administer 10 cc in the morning on an empty stomach 30 minutes before feeding. For the first 20 days, do not breeze, gallop, or undergo rigorous training. Shake 10 times before using.

  • ACTIVE INGREDIENTS

    Argentum Nitricum 200x HPUS
    Allium Sativa 12x HPUS
    Phosphorus 200x HPUS
    Ipecacuanha 30x HPUS 

    Cinnamomum 12x HPUS }

    Pulsatilla 12x HPUS
    Natrum Sulphuricum 12x HPUS
    Rumex Crispus 30x HPUS

  • INACTIVE INGREDIENTS

    Distilled water, Alcohol 3%

  • WARNINGS

    Do not use if seal is broken.
    For Oral Veterinary Use Only.
    Not for use in Horses intended for food.
    If problems persist, contact a veterinarian.
    Keep out of reach of children.

  • OTHER INFORMATION

    Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    STOP 20-PM 
    antimony potassium tartrate, aconitum napellus, phosphorus, potassium carbonate, mercurius solubilis, bryonia alba, paris quadrifolia liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:59517-1730
    Route of AdministrationOral
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B) BRYONIA ALBA ROOT12 [hp_X]  in 1 mL
    PARIS QUADRIFOLIA (UNII: PME3ETQ5WQ) (PARIS QUADRIFOLIA - UNII:PME3ETQ5WQ) PARIS QUADRIFOLIA200 [hp_X]  in 1 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS15 [hp_X]  in 1 mL
    ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE50 [hp_X]  in 1 mL
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS12 [hp_X]  in 1 mL
    POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE12 [hp_X]  in 1 mL
    MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS60 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59517-1730-4200 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/01/2022
    Labeler - Immuvet, Inc. (789097040)
    Registrant - Amino Cell, Inc (099579257)
    Establishment
    NameAddressID/FEIBusiness Operations
    Amino Cell, Inc099579257api manufacture, manufacture
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

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