Label: ANXIETY COMPLEX - ambra grisea, argentum nitricum, aurum metallicum, kali phosphoricum, valeriana officianalis liquid

  • NDC Code(s): 52731-7043-1, 52731-7043-2
  • Packager: Nova Homeopathic Therapeutics, Inc.
  • 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 June 1, 2011

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

  • Purpose:

    Suggested use for one or more of the following symptoms:

    Anxiety, insecurity, fear of tests or exams, dating, public performances, public speaking or shyness.

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  • Usage and Dosage:

    For oral use only.

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  • DOSAGE & ADMINISTRATION

    Adults:

        In Acute Phase:
                12-15 drops, every half hour until relief occurs
        When Relief Occurs:
                12-15 drops, 4-6 times per day

    Children 2-12 years:

                8-10 drops, 4-6 times per day

    Infants 0-24 months:

                3 drops, 4-6 times per day

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  • Warnings:

    Keep out of reach of children.

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  • WARNINGS

    If symptoms persist, consult a physician.

    Do not use if ring on bottom of cap is broken or missing.

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  • Active Ingredients:

    Ambra grisea 6C, Argentum nitricum 12C, Aurum metallicum 12C, Kali phosphoricum 6C, Valeriana officianalis 3C

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  • Inactive Ingredients:

    Alcohol, 20% USP

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  • QUESTIONS

    Manufactured by Nova Homeopathic Therapeutics Inc., Albuquerque, New Mexico USA 87109
    1-800-225-8094

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  • PRINCIPAL DISPLAY PANEL

    Anxiety Complex Product

    Anxiety Complex Product

    Anxiety Complex Bottle Label

    Anxiety Complex Bottle

    Anxiety Complex Box

    Anxiety Complex Box

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  • INGREDIENTS AND APPEARANCE
    ANXIETY COMPLEX 
    ambra grisea, argentum nitricum, aurum metallicum, kali phosphoricum, valeriana officianalis liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:52731-7043
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AMBERGRIS (UNII: XTC0D02P6C) (AMBERGRIS - UNII:XTC0D02P6C) AMBERGRIS 6 [hp_C]  in 1 mL
    SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 12 [hp_C]  in 1 mL
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD 12 [hp_C]  in 1 mL
    POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM PHOSPHATE, DIBASIC 6 [hp_C]  in 1 mL
    VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW) VALERIAN 3 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52731-7043-2 1 in 1 BOX
    1 NDC:52731-7043-1 50 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 06/01/2011
    Labeler - Nova Homeopathic Therapeutics, Inc. (194394540)
    Registrant - Nova Homeopathic Therapeutics, Inc. (194394540)
    Establishment
    Name Address ID/FEI Business Operations
    Nova Homeopathic Therapeutics, Inc. 194394540 manufacture, label, pack
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