Label: G-22- ligustrum vulgare whole solution

  • 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 8, 2022

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  • SPL UNCLASSIFIED SECTION

    NDC 58264-0385-2

  • INDICATIONS

    Heavy menses.

  • INGREDIENTS

    ACTIVE

    Ligustrum vulgare (Privet) 1DH

    INACTIVE

    36.6% alcohol (V/V) Glycerin Macerate

  • SUGGESTED DOSAGE

    One dropper full twice daily.

  • STORAGE AND HANDLING

    SHAKE WELL

  • Warnings

    • Use only if cap seal is unbroken.

    • If pregnant or breastfeeding, ask a healthcare professional before use.

    • Keep this and all medication out of the reach of children.
  • SPL UNCLASSIFIED SECTION

    To be used according to standard homeopathic indications.

  • PRINCIPAL DISPLAY PANEL - 2 FL. OZ. Bottle Label

    DYNAMIC
    NUTRITIONAL

    ASSOCIATES, INC.

    G-22

    LIGUSTRUM
    VULGARE

    GEMMOTHERAPY

    2 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 2 FL. OZ. Bottle Label
  • INGREDIENTS AND APPEARANCE
    G-22 
    ligustrum vulgare whole solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0385
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIGUSTRUM VULGARE WHOLE (UNII: FC604DJ98E) (LIGUSTRUM VULGARE WHOLE - UNII:FC604DJ98E) LIGUSTRUM VULGARE WHOLE1 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0385-259.14 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/01/1990
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/01/1990
    Labeler - DNA Labs, Inc. (031784339)