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Fibromyalgia Relief (Apotheca Company)

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TABLET 125 TABLET in 1 BOTTLE (57520-0582-1) Label Information

Complete Fibromyalgia Relief Information

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENS:  Aconitum napellus 30C, Arsenicum album 30C, Belladonna 30C, Conniinum 30C, Gelsemium sempervirens 30C, Hypericum perforatum 3X, 30C, Kali bichromicum 30C, Lacticum acidum 30C, Phosphoricum acidum 30C, Rhus toxicodendron 30C, Uricum acidum 30C.



  • PURPOSE

    USES:  Temporarily relieves widespread aches, pains, and stiffness.



  • WARNINGS

    WARNINGS:  If pregnant or breastfeeding, ask a health professional before use.

    Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

    OTHER INFORMATION:  Tamper Sealed:  Sealed for your protection.  Do not use if seal is broken or missing.

    Store tightly closed in a cool, dry place (59-86F).

    The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United State.



  • DOSAGE & ADMINISTRATION

    DIRECTIONS:  Adults and children 12 years and above:  Dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician.

    Children under 12 years:  Consult a physician.




  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:  Lactose, Magnesium stearate, Microcrystalline cellulose.



  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.  In case of overdose, get medical help or contact a Poison Control Center right away.



  • INDICATIONS & USAGE

    USES:  Temporarily relieves widespread aches, pains, and stiffness.



  • QUESTIONS


    Dist. by:

    The Magni Group, Inc.

    McKinney, TX 75071 USA

    www.magnilife.com

    1-800645-9199




  • PRINCIPAL DISPLAY PANEL

    MAGNILIFE

    NDC 57520-0582-1

    Homeopathic

    FIBROMYALGIA RELIEF

    For widespread Aches, Pains and Stiffness

    125 Tablets

    Fibromyalgia Relief


  • INGREDIENTS AND APPEARANCE
    FIBROMYALGIA RELIEF 
    aconitum napellus, arsenicum album, belladonna, coniinum, gelsemium sempervirens, hypericum perforatum, kali bichromicum, lacticum acidum, phosphoricum acidum, rhus toxicodendrom, uricum acidum, tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:57520-0582
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS 30 [hp_C]
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC TRIOXIDE - UNII:S7V92P67HO) ARSENIC TRIOXIDE 30 [hp_C]
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 30 [hp_C]
    CONIINE (UNII: C479P32L2D) (CONIINE - UNII:C479P32L2D) CONIINE 30 [hp_C]
    GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM 30 [hp_C]
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM DICHROMATE 30 [hp_C]
    LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (LACTIC ACID, DL- - UNII:3B8D35Y7S4) LACTIC ACID, DL- 30 [hp_C]
    PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 30 [hp_C]
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 30 [hp_C]
    URIC ACID (UNII: 268B43MJ25) (URIC ACID - UNII:268B43MJ25) URIC ACID 30 [hp_C]
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    Color white Score no score
    Shape ROUND (round convex) Size 6mm
    Flavor Imprint Code diamond;
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:57520-0582-1 125 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 06/07/2011
    Labeler - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture