Label: FIBROMYALGIA RELIEF- aconitum napellus, arsenicum album, belladonna, coniinum, gelsemium sempervirens, hypericum perforatum, kali bichromicum tablet

  • NDC Code(s): 43689-0003-1, 43689-0003-2
  • Packager: The Magni Company
  • 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 December 11, 2014

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

  • ACTIVE INGREDIENTS

    Aconitum Napellus 30C, Arsenicum Album 30C, Belladonna 30C, Coniinum 30C, Gelsemium Sempervirens 30C, Hypericum Perforatum 3X, 30C, Kali Bichromicum 30C, Lacticum Acidum 30C, Phosphoricum Acidum 30C, Rhus Toxicodendron 30C, Uricum Acidum 30C.

  • INDICATIONS

    Temporarily relieves widespread aches, pains and stiffness with fatigue.

  • 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.

  • 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 INGREDIENTS

    Lactose, Magnesium Stearate, Microcrystalline Cellulose.

  • KEEP OUT OF REACH OF CHILDREN

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

  • INDICATIONS AND USAGE

    Temporarily relieves widespread aches, pains and stiffness with fatigue.

  • QUESTIONS

    Distributed by:

    The Magni Group, Inc.

    McKinney, TX 75071 USA

    www.magnilife.com    1-800-645-9199

  • PRINCIPAL DISPLAY PANEL

    MAGNILIFE

    since 1999

    Homeopathic

    NDC 43689-0003-2

    FIBROMYALGIA  RELIEF

    For Widespread Aches, Pains and Stiffness with Fatigue

    125 Tablets

    Fibromyalgia Relief

  • INGREDIENTS AND APPEARANCE
    FIBROMYALGIA RELIEF 
    aconitum napellus, arsenicum album, belladonna, coniinum, gelsemium sempervirens, hypericum perforatum, kali bichromicum tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43689-0003
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE30 [hp_C]  in 1 mg
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS30 [hp_C]  in 1 mg
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA30 [hp_C]  in 1 mg
    GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT30 [hp_C]  in 1 mg
    HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM3 [hp_X]  in 1 mg
    CONIINE (UNII: C479P32L2D) (CONIINE - UNII:C479P32L2D) CONIINE30 [hp_C]  in 1 mg
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE30 [hp_C]  in 1 mg
    LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (LACTIC ACID, DL- - UNII:3B8D35Y7S4) LACTIC ACID, DL-30 [hp_C]  in 1 mg
    PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID30 [hp_C]  in 1 mg
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF30 [hp_C]  in 1 mg
    URIC ACID (UNII: 268B43MJ25) (URIC ACID - UNII:268B43MJ25) URIC ACID30 [hp_C]  in 1 mg
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUND (Convex) Size6mm
    FlavorImprint Code ML
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43689-0003-21 in 1 CARTON
    1NDC:43689-0003-1125 mg in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/11/2012
    Labeler - The Magni Company (113501902)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43689-0003) , api manufacture(43689-0003) , label(43689-0003) , pack(43689-0003)