Label: D-133- calcium fluoride, silicon dioxide, tribasic calcium phosphate, calcium sulfate anhydrous, ferrosoferric phosphate, potassium chloride, dibasic potassium phosphate, potassium sulfate, magnesium phosphate, dibasic trihydrate, sodium phosphate, dibasic, heptahydrate, sodium chloride, and sodium sulfate 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 31, 2018

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  • SPL UNCLASSIFIED SECTION

    NDC 58264-0139-1

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  • INDICATIONS

    Mineral imbalances.

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  • INGREDIENTS

    ACTIVE

    Calcarea fluorica 8x, 12x, 30x, Calcarea phosphorica 6x, 12x, 30x, Calcarea sulphurica 6x, 12x, 30x, Ferrum phosphoricum 6x, 12x, 30x, Kalium muriaticum 6x, 12x, 30x, Kalium phosphoricum 6x, 12x, 30x, Kalium sulphuricum 6x, 12x, 30x, Magnesia phosphorica 6x, 12x, 30x, Natrum phosphoricum 6x, 12x, 30x, Natrum muriaticum 6x, 12x, 30x, Natrum sulphuricum 6x, 12x, 30x, Silicea 8x, 12x, 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 133

    HOMEOPATHIC
    STRESS FORMULA

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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  • INGREDIENTS AND APPEARANCE
    D-133 
    calcium fluoride, silicon dioxide, tribasic calcium phosphate, calcium sulfate anhydrous, ferrosoferric phosphate, potassium chloride, dibasic potassium phosphate, potassium sulfate, magnesium phosphate, dibasic trihydrate, sodium phosphate, dibasic, heptahydrate, sodium chloride, and sodium sulfate solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0139
    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
    Silicon dioxide (UNII: ETJ7Z6XBU4) (Silicon dioxide - UNII:ETJ7Z6XBU4) Silicon dioxide 8 [hp_X]  in 1 mL
    Tribasic calcium phosphate (UNII: 91D9GV0Z28) (PHOSPHATE ION - UNII:NK08V8K8HR) Tribasic calcium phosphate 6 [hp_X]  in 1 mL
    Calcium sulfate anhydrous (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB) Calcium sulfate anhydrous 6 [hp_X]  in 1 mL
    Ferrosoferric phosphate (UNII: 91GQH8I5F7) (Ferrosoferric phosphate - UNII:91GQH8I5F7) Ferrosoferric phosphate 6 [hp_X]  in 1 mL
    Potassium chloride (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) Potassium chloride 6 [hp_X]  in 1 mL
    Dibasic potassium phosphate (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR, POTASSIUM CATION - UNII:295O53K152) Dibasic potassium phosphate 6 [hp_X]  in 1 mL
    Potassium sulfate (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152, SULFATE ION - UNII:7IS9N8KPMG) Potassium sulfate 6 [hp_X]  in 1 mL
    Magnesium phosphate, dibasic trihydrate (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) Magnesium phosphate, dibasic trihydrate 6 [hp_X]  in 1 mL
    Sodium phosphate, dibasic, heptahydrate (UNII: 70WT22SF4B) (PHOSPHATE ION - UNII:NK08V8K8HR, SODIUM CATION - UNII:LYR4M0NH37) Sodium phosphate, dibasic, heptahydrate 6 [hp_X]  in 1 mL
    Sodium chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) Sodium chloride 6 [hp_X]  in 1 mL
    Sodium sulfate (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) Sodium sulfate 6 [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:58264-0139-1 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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