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

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

  • ACTIVE INGREDIENT

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


  • PURPOSE

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

  • 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.

  • 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.

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.


  • KEEP OUT OF REACH OF CHILDREN

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


  • INDICATIONS & USAGE

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


  • QUESTIONS

    Enter section text here

  • PRINCIPAL DISPLAY PANEL

    Dr L Advanced HCG Formula

    HOMEOPATHIC

    2 FL OX (60 ml)

    Dr. L Advanced HCG Formula

  • INGREDIENTS AND APPEARANCE
    DR L ADVANCED HCG FORMULA 
    chromium gtf, hypothalamus, hcg, garcinia cambogia, liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57520-0241
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHROMIUM PICOLINATE (UNII: S71T8B8Z6P) (CHROMIUM PICOLINATE - UNII:S71T8B8Z6P) CHROMIUM PICOLINATE13 [hp_C]  in 1 mL
    SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (SUS SCROFA HYPOTHALAMUS - UNII:N6R0856Z79) SUS SCROFA HYPOTHALAMUS13 [hp_C]  in 1 mL
    HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB) (HUMAN CHORIONIC GONADOTROPIN - UNII:20ED16GHEB) HUMAN CHORIONIC GONADOTROPIN34 [hp_C]  in 1 mL
    HYDROXYCITRIC ACID (UNII: 8W94T9026R) (HYDROXYCITRIC ACID - UNII:8W94T9026R) HYDROXYCITRIC ACID 34 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57520-0241-160 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/28/2010
    Labeler - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture