G-19 (ILEX AQUIFOLIUM LEAF) SOLUTION [DNA LABS, INC.]

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G-19 (ILEX AQUIFOLIUM LEAF) SOLUTION [DNA LABS, INC.]
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NDC 58264-0382-2
Set ID 411fd7e6-1a91-4d19-b394-c713c88e2130
Category HUMAN OTC DRUG LABEL
Packager DNA Labs, Inc.
Generic Name
Product Class
Product Number
Application Number
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  • SPL UNCLASSIFIED SECTION

    NDC 58264-0382-2

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  • INDICATIONS

    Support for the kidneys and stomach.

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  • INGREDIENTS

    ACTIVE

    Ilex aquifolium (Holly) 1DH

    INACTIVE

    36.6% alcohol (V/V) Glycerin Macerate

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  • Rx CAUTION

    Federal law prohibits dispensing without a prescription.

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  • SUGGESTED DOSAGE

    One dropper full twice daily.

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  • STORAGE AND HANDLING

    SHAKE WELL

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  • 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.
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  • SPL UNCLASSIFIED SECTION

    To be used according to standard homeopathic indications.

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

    DYNAMIC
    NUTRITIONAL
    ASSOCIATES, INC.

    G-19

    ILEX
    AQUIFOLIUM

    GEMMOTHERAPY

    2 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 2 FL. OZ. Bottle Label
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  • INGREDIENTS AND APPEARANCE
    G-19 
    ilex aquifolium leaf solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0382
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ILEX AQUIFOLIUM LEAF (UNII: 9Z32IEA9F7) (ILEX AQUIFOLIUM LEAF - UNII:9Z32IEA9F7) ILEX AQUIFOLIUM LEAF 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:58264-0382-2 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)
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