Home > Drugs A-Z > Back

Back (Heel Inc.)

Available Formats

Dosage Form Package Information Links
TABLET 100 TABLET in 1 BOTTLE (50114-4262-2) Label Information

Complete Back Information

  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medications out of the reach of children.


  • INDICATIONS AND USAGE

    For the temporary relief of:
    • Lower Back Pain
    • Leg and Hip Pain
    • Neuralgia

  • WARNINGS

    If symptoms persist or worse, a physician should be consulted. As with any drug, if you are pregnant or nursing a baby, seek the advise of a health care professional before using this product.

  • DOSAGE AND ADMINISTRATION

    Adults and Children above 6 years: 1 tablet sublingually or dissolved completely in mouth 3 times daily or as directed by a physician. Infants and children 1/2 the adult dosage.

  • ACTIVE INGREDIENT

    Each 300mg tablet contains as active ingredients; Coloncythis 5X, Gnaphallium polycephalum 5X, Ammonium murlaticum 6X, Gelsenium sempervirens 6X, Rhus toxicodendron 8x, Arsensicum album 10X, Chamomilla 10X 42.86 mg each.

  • INACTIVE INGREDIENT

    Inactive ingredients: Lactose, Magnesium Sterate

  • PURPOSE

    Lower back pain, Leg and hip pain, neuralgia

  • INGREDIENTS AND APPEARANCE
    BACK  
    citrullus colocynthis fruit pulp and pseudognaphalium obtusifolium and ammonium chloride and gelsemium sempervirens root and toxicodendron pubescens leaf and arsenic trioxide and matricaria recutita and tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:50114-4262
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (CITRULLUS COLOCYNTHIS FRUIT PULP - UNII:23H32AOH17) CITRULLUS COLOCYNTHIS FRUIT PULP 5 [hp_X]
    PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW) (PSEUDOGNAPHALIUM OBTUSIFOLIUM - UNII:36XQ854NWW) PSEUDOGNAPHALIUM OBTUSIFOLIUM 5 [hp_X]
    AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4, CHLORIDE ION - UNII:Q32ZN48698) AMMONIUM CHLORIDE 6 [hp_X]
    GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 8 [hp_X]
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC TRIOXIDE - UNII:S7V92P67HO) ARSENIC TRIOXIDE 10 [hp_X]
    MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA 10 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    Color white Score no score
    Shape ROUND (Tablet) Size 9mm
    Flavor Imprint Code BHI;O;M
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:50114-4262-2 100 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 08/30/2007
    Labeler - Heel Inc. (102783016)
    Establishment
    Name Address ID/FEI Business Operations
    Heel Inc. 102783016 manufacture