Label: E-HGH- hgh somatropin liquid

  • NDC Code(s): 50970-002-01, 50970-002-02
  • Packager: AnuMed International LLC
  • Category: HUMAN OTC DRUG LABEL

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 November 29, 2023

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  • ACTIVE INGREDIENTS:

    hGH (Somatropin) 6C, 100C, 200C

  • PURPOSE:

    Improve Sleep, Increase Energy, Anti-Aging Benefits, Increase Lean Muscle

  • USES:

    Reduce fat, Increase lean mass, Improve sleep, Increase energy, Reduce nervousness, Decrease stress and anxiety, Improve sense of well-being

  • WARNINGS:

    Do Not Use

    if tamper evident seal is missing or broken.

    Pregnancy or Breast Feeding

    As with any drug, it you are pregnant or nursing, consult a health care professional before using this product.

    Keep out of the reach of children.

  • DIRECTIONS:

    Adults:Take 5-7 drops 3 times daily. For optimal results place drops under the tongue or swish around mouth for 1 minute. Take as directed by your health care professional.

    Important:Do not consume food or liquid for at least 20 minutes before use.

  • INACTIVE INGREDIENTS:

    Purified Active Water TMwith 20% ethyl alcohol.

  • QUESTIONS OR COMMENTS

    (888) 921-3880

    care@anumed-intl.com

  • SPL UNCLASSIFIED SECTION

    Patent Numbers: 5,629,286; 6,024,734

    Anumed International LLC
    Phoenix Arizona
    www.AnuMed-Intl.com

  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    AnuMed Intl ™

    A Biomed Company

    HEALTHY CELLULAR BALANCE

    e-HGH

    •Improve Sleep                     •Anti-Aging Benefits

    •Increase Energy                   •Increase Lean Muscle

    HOMEOPATHIC FORMULA

    Gold Standard in Homeopathy

    1 oz (30 ml)

    e-HGH Bottle Label
  • INGREDIENTS AND APPEARANCE
    E-HGH 
    hgh somatropin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50970-002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SOMATROPIN (UNII: NQX9KB6PCL) (SOMATROPIN - UNII:NQX9KB6PCL) SOMATROPIN6 [hp_C]  in 200 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50970-002-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product12/31/2023
    2NDC:50970-002-0258 mL in 1 BOTTLE; Type 0: Not a Combination Product12/31/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/01/2011
    Labeler - AnuMed International LLC (961781544)
    Registrant - AnuMed International LLC (961781544)
    Establishment
    NameAddressID/FEIBusiness Operations
    AnuMed International LLC961781544manufacture(50970-002)
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