Label: CARTILAGO ARGENTUM cream

  • 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 January 18, 2024

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  • INDICATIONS & USAGE

    Directions:FOR EXTERNAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Apply to joint(s) several times daily or as needed. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Betula (Silver birch leaves) 3X, Mandragora off. (Mandrake) 3X, Antimonite (Nat. antimony trisulfide) 5X, Aconitum (Monkshood) 6X, Arnica 6X, Argentum met. (Silver) 8X, Cartilago articularis (Bovine cartilage - knee joint) 8X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Sorbic acid, Tea tree oil, Frankincense oil, Myrrh oil, Grapefruit seed extract, Lactose

  • PURPOSE

    Use: Temporary relief of joint pain.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: FOR EXTERNAL USE ONLY.
    Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

  • QUESTIONS

    Questions? Call 866.642.2858
    Made with care by Uriel, East Troy, WI 53120
    shopuriel.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Cartilago Argentum Cream

  • INGREDIENTS AND APPEARANCE
    CARTILAGO ARGENTUM 
    cartilago argentum cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-3260
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB) MANDRAGORA OFFICINARUM ROOT3 [hp_X]  in 1 g
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS6 [hp_X]  in 1 g
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA6 [hp_X]  in 1 g
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER8 [hp_X]  in 1 g
    BOS TAURUS CARTILAGE (UNII: UE77B10IIY) (BOS TAURUS CARTILAGE - UNII:UE77B10IIY) BOS TAURUS CARTILAGE8 [hp_X]  in 1 g
    BETULA PUBESCENS LEAF (UNII: 84SOH0O3OO) (BETULA PUBESCENS LEAF - UNII:84SOH0O3OO) BETULA PUBESCENS LEAF3 [hp_X]  in 1 g
    ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE5 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    FRANKINCENSE OIL (UNII: 67ZYA5T02K)  
    WATER (UNII: 059QF0KO0R)  
    SORBIC ACID (UNII: X045WJ989B)  
    MYRRH OIL (UNII: H74221J5J4)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-3260-560 g in 1 TUBE; Type 0: Not a Combination Product09/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc.043471163manufacture(48951-3260)
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