Label: PURE ORAL HCG - human chorionic gonadotropin liquid 

  • 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 08/10

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

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:  hCG(Human Chorionic Gonadotropin) 13C, 30C, 200C.


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  • PURPOSE

    INDICATIONS:  Supports weight loss.


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  • WARNINGS

    WARNINGS:  If pregnant or breast-feeding, ask a health care 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

    DIRECTIONS:  Adults, 15 drops, under tongue, hold for 30 seconds, then swallow.  This is done 3 times a day, 20 minutes before each meal.  Not intended for children under 12 years of age without physician's care.

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.


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  • QUESTIONS


    Dist. by:

    The Pure Oral hCG Company

    Roseville, CA 95661

    916-607-2500


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  • PRINCIPAL DISPLAY PANEL

    Pure Oral hCG

    Homeopathic

    Pure Oral hCG

    1 fl -z (30 ml)

    Pure Oral hCG

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  • INGREDIENTS AND APPEARANCE
    PURE ORAL HCG 
    hcg, liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:57520-0223
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HUMAN CHORIONIC GONADOTROPIN (HUMAN CHORIONIC GONADOTROPIN) HUMAN CHORIONIC GONADOTROPIN 200 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:57520-0223-1 30 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 08/10/2010
    Labeler - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture
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