G-1 (ABIES ALBA LEAFY TWIG) SOLUTION [DNA LABS, INC.]

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G-1 (ABIES ALBA LEAFY TWIG) SOLUTION [DNA LABS, INC.]
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NDC 58264-0364-2
Set ID ba776ea8-909b-44e0-afcb-1d08e1532897
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 58264-0364-2

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  • INDICATIONS & USAGE

    INDICATIONS

    Late growth, fracture consolidation.

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  • INGREDIENTS

    ACTIVE

    Abies Pectinata (Spruce Fir) 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-1

    ABIES
    PECTINATA

    GEMMOTHERAPY

    2 FL. OZ.

    Principal Display Panel - 2 FL. OZ. Bottle Label
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  • INGREDIENTS AND APPEARANCE
    G-1 
    abies alba leafy twig solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0364
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ABIES ALBA LEAFY TWIG (UNII: CE3G3J56LR) (ABIES ALBA LEAFY TWIG - UNII:CE3G3J56LR) ABIES ALBA LEAFY TWIG 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:58264-0364-2 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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