T-15 (ILEX AQUIFOLIUM WHOLE) SOLUTION [DNA LABS, INC.]

T-15 (ILEX AQUIFOLIUM WHOLE) SOLUTION [DNA LABS, INC.]
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NDC 58264-0260-1
Set ID 361f6453-ebe2-43fb-96c3-1aa232ccfc77
Category HUMAN OTC DRUG LABEL
Packager DNA Labs, Inc.
Generic Name
Product Class
Product Number
Application Number
  • SPL UNCLASSIFIED SECTION

    NDC 58264-0260-1

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  • INDICATIONS

    Hatred, envy, jealousy, suspicion.

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  • INGREDIENTS

    ACTIVE

    Ilex aquifolium 6/8/30x

    INACTIVE

    20% alcohol in purified water.

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  • SUGGESTED DOSAGE

    One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

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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 - 1 FL. OZ. Bottle Label

    DYNAMIC
    NUTRITIONAL

    ASSOCIATES, INC.

    T-15
    HOLLY

    FLOWER ESSENCES

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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  • INGREDIENTS AND APPEARANCE
    T-15 
    ilex aquifolium whole solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0260
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ILEX AQUIFOLIUM WHOLE (UNII: GUI17F6P9J) (ILEX AQUIFOLIUM WHOLE - UNII:GUI17F6P9J) ILEX AQUIFOLIUM WHOLE 30 [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:58264-0260-1 29.57 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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