Label: SHOULDER/ARM COMPLEX- berberis vulgaris, calcarea carbonica, carboneum sulphuratum, causticum, cimicifuga racemosa, cuprum aceticum, ferrum metallicum, kali phosphoricum, ruta graveolens, silicea, spigelia anthelmia, spiraea ulmaria liquid

  • Category: HUMAN OTC DRUG LABEL

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

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  • Purpose:

    Suggested use for one or more of the following symptoms:

    Aching, tightness, stiffness in muscles or joints of neck, shoulders, arms, hands or fingers.

  • Usage and Dosage:

    For oral use only.

  • 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

  • Warnings:

    Keep out of reach of children

  • WARNINGS

    If symptoms persist, consult a physician.

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

  • Active Ingredients:

    Berberis vulgaris 4X, Calcarea carbonica 8X, Carboneum sulphuratum 6X, Causticum 6X, Cimicifuga racemosa 6X, Cuprum aceticum 4X, Ferrum metallicum 8X, Kali phosphoricum 8X, Ruta graveolens 4X, Silicea 8X, Spigelia anthelmia 4X, Spiraea ulmaria 4X

  • Inactive Ingredients:

    Alcohol, 20% USP

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    Shoulder/Arm Complex Product


    Shoulder/Arm Complex Product

    Shoulder/Arm Complex Bottle Label

    Shoulder/Arm Complex Bottle

    Shoulder/Arm Complex Box


    Shoulder/Arm Complex Box




  • INGREDIENTS AND APPEARANCE
    SHOULDER/ARM COMPLEX 
    berberis vulgaris, calcarea carbonica, carboneum sulphuratum, causticum, cimicifuga racemosa, cuprum aceticum, ferrum metallicum, kali phosphoricum, ruta graveolens, silicea, spigelia anthelmia, spiraea ulmaria liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52731-7022
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK4 [hp_X]  in 1 mL
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE8 [hp_X]  in 1 mL
    CARBON DISULFIDE (UNII: S54S8B99E8) (CARBONATE ION - UNII:7UJQ5OPE7D) CARBON DISULFIDE6 [hp_X]  in 1 mL
    CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) CAUSTICUM6 [hp_X]  in 1 mL
    BLACK COHOSH (UNII: K73E24S6X9) (BLACK COHOSH - UNII:K73E24S6X9) BLACK COHOSH6 [hp_X]  in 1 mL
    CUPRIC ACETATE (UNII: 39M11XPH03) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC ACETATE4 [hp_X]  in 1 mL
    IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON8 [hp_X]  in 1 mL
    POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM PHOSPHATE, DIBASIC8 [hp_X]  in 1 mL
    RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP4 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE8 [hp_X]  in 1 mL
    SPIGELIA ANTHELMIA (UNII: WYT05213GE) (SPIGELIA ANTHELMIA - UNII:WYT05213GE) SPIGELIA ANTHELMIA4 [hp_X]  in 1 mL
    FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) (FILIPENDULA ULMARIA ROOT - UNII:997724QNDS) FILIPENDULA ULMARIA ROOT4 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52731-7022-21 in 1 BOX
    1NDC:52731-7022-150 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/01/2011
    Labeler - Nova Homeopathic Therapeutics, Inc. (194394540)
    Registrant - Nova Homeopathic Therapeutics, Inc. (194394540)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nova Homeopathic Therapeutics, Inc.194394540manufacture, label, pack
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