Label: L DOPA PHENOLIC- levodopa 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 02/13

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

  • ACTIVE INGREDIENTS

    L Dopa 6X, 12X, 30X, 12C, 30C

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  • INDICATIONS

    To be used according to standarad homeopathic indications.

    **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

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  • WARNINGS

    If pregnant or breast-feeding, 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.

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  • DIRECTIONS

    Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

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  • INACTIVE INGREDIENTS

    Demineralized water, 20% Ethanol.

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  • KEEP OUT OF REACH OF CHILDREN

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

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  • INDICATIONS AND USAGE

    To be used according to standarad homeopathic indications.

    **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

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  • QUESTIONS

    Dist. by Energique, Inc.

    201 Apple Blvd

    Woodbine, IA 51579

    800-869-8078

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  • PRINCIPAL DISPLAY PANEL

    ENERGIQUE

    since 1987

    HOMEOPATHIC REMEDY

    L DOPA

    PHENOLIC

    1 fl. oz. (30 ml)

    L Dopa Phenolic

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  • INGREDIENTS AND APPEARANCE
    L DOPA PHENOLIC 
    l dopa liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:44911-0035
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LEVODOPA (LEVODOPA) LEVODOPA 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:44911-0035-1 30 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 02/19/2013
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(44911-0035)
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