Label: D17- naja naja whole, scrophularia nodosa, lactic acid, dl-, and radium bromide 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 January 30, 2018

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  • SPL UNCLASSIFIED SECTION

    NDC 58264-0017-1

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  • INDICATIONS

    Regenerator of diseased tissue.

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  • ACTIVE INGREDIENT

    INGREDIENTS

    Scrophularia nodosa 2x, Acidum lactium 4x, Radium bromatum 30x, Naja tripudians 30x, 24% alcohol in purified water.

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  • RX CAUTION

    Federal law prohibits dispensing without a prescription.

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  • SUGGESTED DOSAGE

    One dropper full under the tongue two times daily. In acute conditions 5-10 drops under the tongue every 20-30 minutes.

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  • STORAGE AND HANDLING

    SHAKE WELL

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  • Warnings

    • Use only if cap seal is unbroken.

    • As with drugs if you are pregnant or nursing a baby seek professional advice before using this product.

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

    To be used according to standard homeopathic indications.

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  • PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label

    DYNAMIC
    NUTRITIONAL

    ASSOCIATES, INC.

    D 17

    HOMEOPATHIC FORMULA

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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  • INGREDIENTS AND APPEARANCE
    D17 
    naja naja whole, scrophularia nodosa, lactic acid, dl-, and radium bromide solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0017
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Naja Naja Whole (UNII: D279BDR31E) (Naja Naja Whole - UNII:D279BDR31E) Naja Naja Whole 30 [hp_X]  in 1 mL
    Scrophularia nodosa (UNII: 7H443NUB2T) (Scrophularia nodosa - UNII:7H443NUB2T) Scrophularia nodosa 2 [hp_X]  in 1 mL
    Lactic Acid, DL- (UNII: 3B8D35Y7S4) (Lactic Acid, DL- - UNII:3B8D35Y7S4) Lactic Acid, DL- 4 [hp_X]  in 1 mL
    Radium bromide (UNII: R74O7T8569) (Radium Cation - UNII:05456MVL7T) Radium bromide 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:58264-0017-1 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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