G-22 (LIGUSTRUM VULGARE WHOLE) SOLUTION [DNA LABS, INC.]

G-22 (LIGUSTRUM VULGARE WHOLE) SOLUTION [DNA LABS, INC.]
PDF | XML

NDC 58264-0385-2
Set ID d30d72f9-458d-4daa-8481-6cae8ad49b9f
Category HUMAN OTC DRUG LABEL
Packager DNA Labs, Inc.
Generic Name
Product Class
Product Number
Application Number
  • SPL UNCLASSIFIED SECTION

    NDC 58264-0385-2

    Close
  • INDICATIONS

    Heavy menses.

    Close
  • INGREDIENTS

    ACTIVE

    Ligustrum vulgare (Privet) 1DH

    INACTIVE

    36.6% alcohol (V/V) Glycerin Macerate

    Close
  • SUGGESTED DOSAGE

    One dropper full twice daily.

    Close
  • STORAGE AND HANDLING

    SHAKE WELL

    Close
  • 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.
    Close
  • SPL UNCLASSIFIED SECTION

    To be used according to standard homeopathic indications.

    Close
  • 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
    Close
  • INGREDIENTS AND APPEARANCE
    G-22 
    ligustrum vulgare whole solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0385
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIGUSTRUM VULGARE WHOLE (UNII: FC604DJ98E) (LIGUSTRUM VULGARE WHOLE - UNII:FC604DJ98E) LIGUSTRUM VULGARE WHOLE 1 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:58264-0385-2 59.14 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/01/1990
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    UNAPPROVED HOMEOPATHIC 01/01/1990
    Labeler - DNA Labs, Inc. (031784339)
    Close

Related Drugs