Label: AM-7- strychnos nux-vomica seed, sodium phosphate, dibasic, heptahydrate, and bufo bufo whole 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 March 23, 2018

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  • SPL UNCLASSIFIED SECTION

    NDC 58264-0346-1

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  • INDICATIONS

    Regulates energy flow in the liver meridian.

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  • INGREDIENTS

    ACTIVE

    Nux vomica 8x, Natrum phosphoricum 8x, Bufo rana 12x

    INACTIVE

    20% alcohol in purified water.

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  • SUGGESTED DOSAGE

    5 to 10 drops twice a day, meridian energy excess 1 to 5 drops t.i.d, meridian lacking in energy 10 to 20 drops t.i.d.

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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.

    AM-7
    LIVER

    ACUPUNCTURE MERIDIAN

    1 FL. OZ.

    PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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  • INGREDIENTS AND APPEARANCE
    AM-7 
    strychnos nux-vomica seed, sodium phosphate, dibasic, heptahydrate, and bufo bufo whole solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0346
    Route of Administration SUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Strychnos nux-vomica seed (UNII: 269XH13919) (Strychnos nux-vomica seed - UNII:269XH13919) Strychnos nux-vomica seed 8 [hp_X]  in 1 mL
    Sodium Phosphate, Dibasic, Heptahydrate (UNII: 70WT22SF4B) (PHOSPHATE ION - UNII:NK08V8K8HR, SODIUM CATION - UNII:LYR4M0NH37) Sodium Phosphate, Dibasic, Heptahydrate 8 [hp_X]  in 1 mL
    BUFO BUFO WHOLE (UNII: DP1U601YQS) (BUFO BUFO WHOLE - UNII:DP1U601YQS) BUFO BUFO WHOLE 12 [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:58264-0346-1 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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