Label: ACETYLCHOLINE CHLORIDE PHENOLIC - acetylcholine chloride liquid

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

Drug Label Information

Updated 09/10

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:  Acetylcholine Chloride 6X, 12X, 30X, 12C, 30C.

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  • PURPOSE

    INDICATIONS:  For temporary relief of dizziness, chest congestion with mild constriction, fatigue, cough, headaches, forgetfulness and drowsiness.


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  • WARNINGS

    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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  • DOSAGE & ADMINISTRATION

    SUGGESTED USE:  Adults and children 5 to 10 drops orally, 1 time 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 INGREDIENT

    INACTIVE INGREDIENTS:  Demineralized water, 20% Ethanol


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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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  • INDICATIONS & USAGE

    INDICATIONS:  For temporary relief of dizziness, chest congestion with mild constriction, fatigue, cough, headaches, forgetfulness and drowsiness.


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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

    ACETLYCHOLINE CHLORIDE PHENOLIC

    Homeopathic Remedy

    1 fl. oz. (30 ml)

    Acetlycholine Chloride Phenolic

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  • INGREDIENTS AND APPEARANCE
    ACETYLCHOLINE CHLORIDE PHENOLIC 
    acetylcholine chloride, liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:57520-0401
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R) (ACETYLCHOLINE - UNII:N9YNS0M02X) ACETYLCHOLINE CHLORIDE 30 [hp_C]  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:57520-0401-1 30 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 05/07/2010
    Labeler - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture
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