Label: DR L ADVANCED HCG FORMULA - chromium gtf, hypothalamus, hcg, garcinia cambogia, 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 October 28, 2010

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:  Chromium GTF 13C, Hypothalamus 13C, Human Chorionic Gonadotropin (HCG) 13C, 21C, 34C, Garcinia cambogia 34C.


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  • PURPOSE

    INDICATIONS:  For temporary relief of symptoms related to obesity and metabolism.

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  • WARNINGS

    WARNINGS:  Keep out of reach of children.  In case of overdose, contact physician or Poison Control Center right away.

    If pregnant or breast-feeding, seek advice of a health professional before use.

    Tamper seal:  "Sealed for your protection."  Do not use if seal is broken or missing.

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  • DOSAGE & ADMINISTRATION

    DIRECTIONS:  Tap bottom of bottle 40 times before each use.  15 drops 2 times daily or 10 drops 3 times daily under tongue, hold 30 seconds and swallow.  Consult a physician for use in children under 12 years of age.

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.


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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.  In case of overdose, contact physician or Poison Control Center right away.


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  • INDICATIONS & USAGE

    INDICATIONS:  For temporary relief of symptoms related to obesity and metabolism.


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  • QUESTIONS

    Enter section text here

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  • PRINCIPAL DISPLAY PANEL

    Dr L Advanced HCG Formula

    HOMEOPATHIC

    2 FL OX (60 ml)

    Dr. L Advanced HCG Formula

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  • INGREDIENTS AND APPEARANCE
    DR L ADVANCED HCG FORMULA 
    chromium gtf, hypothalamus, hcg, garcinia cambogia, liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:57520-0241
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHROMIUM PICOLINATE (UNII: S71T8B8Z6P) (CHROMIUM PICOLINATE - UNII:S71T8B8Z6P) CHROMIUM PICOLINATE 13 [hp_C]  in 1 mL
    SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (SUS SCROFA HYPOTHALAMUS - UNII:N6R0856Z79) SUS SCROFA HYPOTHALAMUS 13 [hp_C]  in 1 mL
    HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB) (HUMAN CHORIONIC GONADOTROPIN - UNII:20ED16GHEB) HUMAN CHORIONIC GONADOTROPIN 34 [hp_C]  in 1 mL
    HYDROXYCITRIC ACID (UNII: 8W94T9026R) (HYDROXYCITRIC ACID - UNII:8W94T9026R) HYDROXYCITRIC ACID 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:57520-0241-1 60 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 10/28/2010
    Labeler - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture
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