Label: BONE AND JOINT REMEDY- calcarea carbonica, calcarea fluorica, calcarea phosphorica, equisetum hyemale, hekla lava, phosphorus, silicea liquid

  • 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 February 16, 2018

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  • DOSAGE & ADMINISTRATION

    Directions: Spray 3 times directly into mouth under your tongue. Take 3 times daily. One bottle lasts approximately one month. For maximum benefits, take daily until symptoms relieved.

  • WARNINGS

    Warnings: Stop use and ask a doctor, if symptoms persist or worsen. If pregnant or breast-feeding, consult a healthcare professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OTHER SAFETY INFORMATION

    Other: Do not use if safety seal is broken or missing.

  • PURPOSE

    Uses: ​May help to strengthen bones and relieve joint pain and back pain.​

  • ACTIVE INGREDIENT

    Ingredients: Calcarea carbonica, Calcarea fluorica, Calcarea phosphorica, Equisetum hyemale, Hekla lava, Phosphorus, Silicea.

    Equal volumes of each ingredient in 10X, 30X, 1LM potencies.

  • INACTIVE INGREDIENT

    Inactive ingredients: Bio-Energetically enhanced pure water, Carya ovata bark extract (hickory), citrus extract, Lonicera japonica (honeysuckle), polylysine (natural ferment), steviol glycoside (stevia)

  • INDICATIONS & USAGE

    Uses: May help to:

    • strengthen bones
    • relieve joint pain
    • back pain
  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    BONE AND JOINT REMEDY 
    calcarea carbonica, calcarea fluorica, calcarea phosphorica, equisetum hyemale, hekla lava, phosphorus, silicea liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53852-0012
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE10 [hp_X]  in 59 mL
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE10 [hp_X]  in 59 mL
    TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION10 [hp_X]  in 59 mL
    EQUISETUM HYEMALE (UNII: 59677RXH25) (EQUISETUM HYEMALE - UNII:59677RXH25) EQUISETUM HYEMALE10 [hp_X]  in 59 mL
    HEKLA LAVA (UNII: C21158IIRK) (HEKLA LAVA - UNII:C21158IIRK) HEKLA LAVA10 [hp_X]  in 59 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS10 [hp_X]  in 59 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE10 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARYA OVATA BARK (UNII: X765CF609L)  
    CITRUS BIOFLAVONOIDS (UNII: BD70459I50)  
    LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)  
    POLYEPSILON-LYSINE (4000 MW) (UNII: WB0M8X4TWR)  
    REBAUDIOSIDE A (UNII: B3FUD0528F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53852-0012-259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/16/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic02/16/2018
    Labeler - Living Well Remedies, LLC (022609201)
    Registrant - Living Well Remedies, LLC (022609201)
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