Label: D-120- calcium fluoride, bismuth subnitrate, zinc, mercuric chloride, toxicodendron pubescens leaf, antimony trisulfide, barium carbonate, echinacea angustifolia, iodine, phosphoric acid, potassium carbonate, dibasic potassium phosphate, and thuja occidentalis leafy twig 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 July 26, 2018

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    NDC 58264-0126-1

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  • INDICATIONS

    Loose teeth, sore gums.

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  • INGREDIENTS

    ACTIVE

    Calcarea fluorica 8x, 12x, Bismuthum 6x, 12x, Zincum metallicum 8x, Mercurius corrosivus 6x, 30x, Rhus toxicodendron 4x, 30x, Antimonium crudum 8x, 12x, Baryta carbonica 8x, 30x, Echinacea angustifolia 4x, 12x, Iodium 4x, 30x, Acidum phosphoricum 4x, 6x, Kalium carbonicum 6x, 30x, Kalium phosphoricum 4x, 12x, Thuja occidentalis 4x, 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.

    D 120

    HOMEOPATHIC
    STRESS FORMULA

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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  • INGREDIENTS AND APPEARANCE
    D-120 
    calcium fluoride, bismuth subnitrate, zinc, mercuric chloride, toxicodendron pubescens leaf, antimony trisulfide, barium carbonate, echinacea angustifolia, iodine, phosphoric acid, potassium carbonate, dibasic potassium phosphate, and thuja occidentalis leafy twig solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0126
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Calcium fluoride (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) Calcium fluoride 8 [hp_X]  in 1 mL
    BISMUTH SUBNITRATE (UNII: H19J064BA5) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBNITRATE 6 [hp_X]  in 1 mL
    Zinc (UNII: J41CSQ7QDS) (Zinc - UNII:J41CSQ7QDS) Zinc 8 [hp_X]  in 1 mL
    Mercuric Chloride (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) Mercuric Chloride 6 [hp_X]  in 1 mL
    Toxicodendron pubescens leaf (UNII: 6IO182RP7A) (Toxicodendron pubescens leaf - UNII:6IO182RP7A) Toxicodendron pubescens leaf 4 [hp_X]  in 1 mL
    Antimony trisulfide (UNII: F79059A38U) (Antimony trisulfide - UNII:F79059A38U, ANTIMONY CATION (3+) - UNII:069647RPT5) Antimony trisulfide 8 [hp_X]  in 1 mL
    Barium carbonate (UNII: 6P669D8HQ8) (BARIUM CATION - UNII:V645272HLN) Barium carbonate 8 [hp_X]  in 1 mL
    Echinacea angustifolia (UNII: VB06AV5US8) (Echinacea angustifolia - UNII:VB06AV5US8) Echinacea angustifolia 4 [hp_X]  in 1 mL
    Iodine (UNII: 9679TC07X4) (Iodine - UNII:9679TC07X4) Iodine 4 [hp_X]  in 1 mL
    Phosphoric acid (UNII: E4GA8884NN) (Phosphoric acid - UNII:E4GA8884NN) Phosphoric acid 4 [hp_X]  in 1 mL
    Potassium carbonate (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) Potassium carbonate 6 [hp_X]  in 1 mL
    Dibasic potassium phosphate (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR, POTASSIUM CATION - UNII:295O53K152) Dibasic potassium phosphate 4 [hp_X]  in 1 mL
    Thuja occidentalis Leafy twig (UNII: 1NT28V9397) (Thuja occidentalis Leafy twig - UNII:1NT28V9397) Thuja occidentalis Leafy twig 4 [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:58264-0126-1 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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