Label: MENADIONE- menadione liquid 

  • Label RSS
  • 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 10/13

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

  • ACTIVE INGREDIENTS:

    Menadione 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

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  • INDICATIONS:

    For temporary relief of symptoms related to Menadione sensitivity including colitis, diarrhea, gas, abdominal cramps, rash, headache, varicose veins, and arthritis.

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  • WARNINGS:

    ​Keep out of reach of children.​ In case of overdose, contact a physician or Poison Control Center right away.

    ​If pregnant or breast-feeding,​ ask a health professional before use.

    Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

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  • KEEP OUT OF REACH OF CHILDREN:

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

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  • DIRECTIONS:

    1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

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  • INDICATIONS:

    For temporary relief of symptoms related to Menadione sensitivity including colitis, diarrhea, gas, abdominal cramps, rash, headache, varicose veins, and arthritis.

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  • INACTIVE INGREDIENTS:

    Demineralized Water, 25% Ethanol

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  • QUESTIONS:

    Dist. By: Deseret Biologicals, Inc.

    469 Parkland Drive

    Sandy, UT 84070    www.desbio.com

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  • PACKAGE DISPLAY LABEL:

    ​DESBIO

    NDC 43742-0299-1

    HOMEOPATHIC

    MENADIONE

    1 FL OZ (30 ml)

    Menadione

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  • INGREDIENTS AND APPEARANCE
    MENADIONE 
    menadione liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:43742-0299
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MENADIONE (MENADIONE) MENADIONE 6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43742-0299-1 30 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 10/03/2013
    Labeler - Deseret Biologicals (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(43742-0299), api manufacture(43742-0299), label(43742-0299), pack(43742-0299)
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