Label: CARTILAGO ARGENTUM JOINT SUPPORT - mandragora officinarum root betula pendula leaf aconitum napellus root arnica montana silver pellet

  • 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 31, 2009

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

  • Purpose

    Uses: Temporarily relieves symptoms of aches and pains in joints.

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  • Dosage & Administration

    Directions: Dissolve under tongue 3-4 times daily. Age 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: ask a doctor.

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  • OTC-Active Ingredient

    Active Ingredients: Betula e fol. 5x, Mandragora off. e rad. 5X, Aconitum e tub. 6X, Arnica e pl. tota 6X, Argentum metallicum 8X, all HPUS.

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  • Inactive Ingredient

    Inactive Ingredients: Sucrose, Antimonite 6X, Cartilago articularis 6X.

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  • Keep out of reach of children

    KEEP OUT OF REACH OF CHILDREN.

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  • Do not use section

    Warnings:  Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

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  • Ask doctor section

    Consult a doctor if symptoms are serious or persist for 3 days, if you are diabetic or intolerant of sugar.

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  • Pregnancy or breast feeding section

    If you are pregnant or nursing, consult a doctor before use.

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  • Questions section

    Questions? Uriel Pharmacy

    866 642-2858  East Troy, WI 53120 

    www.urielpharmacy.com

    NDC 48951-3037-2

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  • Principal Display Panel

    Cartilago Argentum

    Joint Support

    Homeopathic Pellets

    net wt. 1 oz.

    cartilago argentum pellets bottle label

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  • INGREDIENTS AND APPEARANCE
    CARTILAGO ARGENTUM JOINT SUPPORT 
    mandragora officinarum root betula pendula leaf aconitum napellus root arnica montana silver pellet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-3037
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB) MANDRAGORA OFFICINARUM ROOT 5 [hp_X]
    BETULA PENDULA LEAF (UNII: 5HW39H9KDH) (BETULA PENDULA LEAF - UNII:5HW39H9KDH) BETULA PENDULA LEAF 5 [hp_X]
    ACONITUM NAPELLUS ROOT (UNII: KPD2N7348X) (ACONITUM NAPELLUS ROOT - UNII:KPD2N7348X) ACONITUM NAPELLUS ROOT 6 [hp_X]
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 6 [hp_X]
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 8 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    Color white (white) Score no score
    Shape ROUND (round) Size 3mm
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:48951-3037-2 1350 in 1 BOTTLE, GLASS
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 09/01/2009
    Labeler - Uriel Pharmacy Inc (043471163)
    Establishment
    Name Address ID/FEI Business Operations
    Uriel Pharmacy Inc 043471163 manufacture
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