Label: NERVE PRO HP- plantago major, xanthoxylum fraxineum, colocynthis, magnesia phosphorica, agaricus muscarius, hypericum perforatum, argentum nitricum, carboneum sulphuratum, curare, thallium metallicum 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 May 14, 2019

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

  • ACTIVE INGREDIENTS:

    (in each drop): 7.14% of Agaricus Muscarius 12X, 30X, 200X, Argentum Nitricum 30X, Carboneum Sulphuratum 30X, Colocynthis 12X, Curare 30X, Hypericum Perforatum 12X, 30X, 200X, Magnesia Phosphorica 12X, Plantago Major 6X, Thallium Metallicum 30X, Xanthoxylum Fraxineum 6X.

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  • INDICATIONS:

    May temporarily relieve symptoms of tingling, burning, and numbness in the hands and feet.**

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

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  • WARNINGS:

    If 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.

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  • 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.

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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 for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

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  • INDICATIONS:

    May temporarily relieve symptoms of tingling, burning, and dumbness in the hands and feet.**

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

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  • INACTIVE INGREDIENTS:

    Demineralized water, 20% Ethanol.

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  • QUESTIONS:

    Dist. by Energique, Inc.
    201 Apple Blvd.
    Woodbine, IA 51579 800.868.8078

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  • PACKAGE LABEL DISPLAY:

    ENERGIQUE
    SINCE 1987
    HOMEOPATHIC REMEDY
    NERVE PRO

    HP
    1 fl. oz. (30 ml)

    Nerve Pro HP

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  • INGREDIENTS AND APPEARANCE
    NERVE PRO  HP
    plantago major, xanthoxylum fraxineum, colocynthis, magnesia phosphorica, agaricus muscarius, hypericum perforatum, argentum nitricum, carboneum sulphuratum, curare, thallium metallicum liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0495
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PLANTAGO MAJOR (UNII: W2469WNO6U) (PLANTAGO MAJOR - UNII:W2469WNO6U) PLANTAGO MAJOR 6 [hp_X]  in 1 mL
    ZANTHOXYLUM AMERICANUM BARK (UNII: A4KL1HMZ7T) (ZANTHOXYLUM AMERICANUM BARK - UNII:A4KL1HMZ7T) ZANTHOXYLUM AMERICANUM BARK 6 [hp_X]  in 1 mL
    CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (CITRULLUS COLOCYNTHIS FRUIT PULP - UNII:23H32AOH17) CITRULLUS COLOCYNTHIS FRUIT PULP 12 [hp_X]  in 1 mL
    MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X]  in 1 mL
    AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (AMANITA MUSCARIA FRUITING BODY - UNII:DIF093I037) AMANITA MUSCARIA FRUITING BODY 12 [hp_X]  in 1 mL
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM 12 [hp_X]  in 1 mL
    SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 30 [hp_X]  in 1 mL
    CARBON DISULFIDE (UNII: S54S8B99E8) (CARBON DISULFIDE - UNII:S54S8B99E8) CARBON DISULFIDE 30 [hp_X]  in 1 mL
    TUBOCURARINE CHLORIDE (UNII: 900961Z8VR) (TUBOCURARINE - UNII:W9YXS298BM) TUBOCURARINE CHLORIDE 30 [hp_X]  in 1 mL
    THALLIUM (UNII: AD84R52XLF) (THALLIUM - UNII:AD84R52XLF) THALLIUM 30 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:44911-0495-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/14/2019
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 05/14/2019
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(44911-0495) , api manufacture(44911-0495) , label(44911-0495) , pack(44911-0495)
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