Label: BIOTOX PEST DETOX- glyphosate liquid

  • 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 March 17, 2021

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

  • ACTIVE INGREDIENTS:

    Glyphosate 6C, 12C, 30C, 60C, 200C.

  • INDICATIONS:

    Difficulty breathing, diarrhea, dizziness, drowsiness, vomiting, stomach cramps, nausea, abdominal pain, indigestion, feeling of high blood pressure. 

  • WARNINGS:

    If you are pregnant or breastfeeding, ask a health professional before use.

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

    Do not use if tamper evident seal is broken or missing.

    Store in a cool, dry place.

  • KEEP OUT OF REACH OF CHILDREN:

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS:

    5 drops orally 3 times per day, 5 days per week, or according to provider recommendations. Consult a physician for use in children under 12 years of age.

  • INDICATIONS:

    Difficulty breathing, diarrhea, dizziness, drowsiness, vomiting, stomach cramps, nausea, abdominal pain, indigestion, feeling of high blood pressure.

  • INACTIVE INGREDIENTS:

    Demineralized Water, 25% Organic Ethanol

  • QUESTIONS:

    MFD FOR:

    The Wellness Center for

    Research and Education, Inc.

    1237 S. Victoria Ave. Suite 169

    Oxnard, CA 93035 

  • PACKAGE LABEL DISPLAY:

    Dr. Theresa Dale's

    NDC 50181-0060-1

    Homeopathic

    BioTox

    Pest Detox

    1 fl oz (30 ml)

    BioTox Pest Detox

  • INGREDIENTS AND APPEARANCE
    BIOTOX PEST DETOX 
    glyphosate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50181-0060
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYPHOSATE (UNII: 4632WW1X5A) (GLYPHOSATE - UNII:4632WW1X5A) GLYPHOSATE6 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50181-0060-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product03/16/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/16/2018
    Labeler - The Wellness Center For Research and Education (832363993)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(50181-0060) , api manufacture(50181-0060) , label(50181-0060) , pack(50181-0060)