Label: HCG CORD - hcg (human chorionic gonadotropin) spray

  • 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 June 29, 2010

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:  HCG(Human Chorionic Gonadotropin) 13C, 21C, 34C.

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  • PURPOSE

    INDICATIONS:  Supports weight loss by regulating male and female hormone functions and also by suppressing ravenous appetite.

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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 spray twice under the tongue one time daily.  Not recommended for children.

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:  Demineralized water, 20% Ethanol

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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

    HCG CORD

    Homeopathic Remedy

    1 fl. oz. (30 ml)

    HCG Cord

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  • INGREDIENTS AND APPEARANCE
    HCG CORD 
    hcg (human chorionic gonadotropin) spray
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:57520-0341
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB) (HUMAN CHORIONIC GONADOTROPIN - UNII:20ED16GHEB) HUMAN CHORIONIC GONADOTROPIN 34 [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:57520-0341-1 30 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 04/29/2010
    Labeler - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture
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