D-120 (CALCIUM FLUORIDE, BISMUTH SUBNITRATE, ZINC, MERCURIC CHLORIDE, TOXICODENDRON PUBESCENS LEAF, ANTIMONY TRISULFIDE, BARIUM CARBONATE, ECHINACEA ANGUSTIFOLIA, IODINE, PHOSPHORIC ACID, POT

D-120 (CALCIUM FLUORIDE, BISMUTH SUBNITRATE, ZINC, MERCURIC CHLORIDE, TOXICODENDRON PUBESCENS LEAF, ANTIMONY TRISULFIDE, BARIUM CARBONATE, ECHINACEA ANGUSTIFOLIA, IODINE, PHOSPHORIC ACID, POT
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NDC 58264-0126-1
Set ID 9525c016-f0dd-43fd-a4e9-062075107eec
Category HUMAN OTC DRUG LABEL
Packager DNA Labs, Inc.
Generic Name
Product Class
Product Number
Application Number
  • SPL UNCLASSIFIED SECTION

    NDC 58264-0126-1

  • INDICATIONS

    Loose teeth, sore gums.

  • 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.

  • SUGGESTED DOSAGE

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

  • STORAGE AND HANDLING

    SHAKE WELL

  • 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.
  • SPL UNCLASSIFIED SECTION

    To be used according to standard homeopathic indications.

  • 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
  • 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 TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0126
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Calcium fluoride (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) Calcium fluoride8 [hp_X]  in 1 mL
    BISMUTH SUBNITRATE (UNII: H19J064BA5) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBNITRATE6 [hp_X]  in 1 mL
    Zinc (UNII: J41CSQ7QDS) (Zinc - UNII:J41CSQ7QDS) Zinc8 [hp_X]  in 1 mL
    Mercuric Chloride (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) Mercuric Chloride6 [hp_X]  in 1 mL
    Toxicodendron pubescens leaf (UNII: 6IO182RP7A) (Toxicodendron pubescens leaf - UNII:6IO182RP7A) Toxicodendron pubescens leaf4 [hp_X]  in 1 mL
    Antimony trisulfide (UNII: F79059A38U) (Antimony trisulfide - UNII:F79059A38U, ANTIMONY CATION (3+) - UNII:069647RPT5) Antimony trisulfide8 [hp_X]  in 1 mL
    Barium carbonate (UNII: 6P669D8HQ8) (BARIUM CATION - UNII:V645272HLN) Barium carbonate8 [hp_X]  in 1 mL
    Echinacea angustifolia (UNII: VB06AV5US8) (Echinacea angustifolia - UNII:VB06AV5US8) Echinacea angustifolia4 [hp_X]  in 1 mL
    Iodine (UNII: 9679TC07X4) (Iodine - UNII:9679TC07X4) Iodine4 [hp_X]  in 1 mL
    Phosphoric acid (UNII: E4GA8884NN) (Phosphoric acid - UNII:E4GA8884NN) Phosphoric acid4 [hp_X]  in 1 mL
    Potassium carbonate (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) Potassium carbonate6 [hp_X]  in 1 mL
    Dibasic potassium phosphate (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR, POTASSIUM CATION - UNII:295O53K152) Dibasic potassium phosphate4 [hp_X]  in 1 mL
    Thuja occidentalis Leafy twig (UNII: 1NT28V9397) (Thuja occidentalis Leafy twig - UNII:1NT28V9397) Thuja occidentalis Leafy twig4 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alcohol (UNII: 3K9958V90M)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58264-0126-129.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/01/1990
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED HOMEOPATHIC01/01/1990
    Labeler - DNA Labs, Inc. (031784339)

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