Label: MANDRAGORA RHEUM 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 November 22, 2023

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  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • DOSAGE & ADMINISTRATION

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

  • ACTIVE INGREDIENT

    Active Ingredients: Mandragora (Mandrake) 3X, Taraxacum (Dandelion) 3X, Argentum met. (Silver) 6X, Collagen (Bovine collagen) 6X, Formica (Red wood ant) 6X, Pancreas (Bovine pancreas) 6X, Periosteum (Bovine periosteum) 8X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Organic sucrose

  • PURPOSE

    Use: Temporary relief of sore joints.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

  • QUESTIONS

    Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 shopuriel.com

  • PRINCIPAL DISPLAY PANEL

    Mandragora Rheum Pellets

  • INGREDIENTS AND APPEARANCE
    MANDRAGORA RHEUM 
    mandragora rheum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-7016
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB) MANDRAGORA OFFICINARUM ROOT3 [hp_X]
    TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C) (TARAXACUM PALUSTRE ROOT - UNII:GCZ4W7077C) TARAXACUM PALUSTRE ROOT3 [hp_X]
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER6 [hp_X]
    BOVINE TYPE I COLLAGEN (UNII: FHJ3ATL51C) (BOVINE TYPE I COLLAGEN - UNII:FHJ3ATL51C) BOVINE TYPE I COLLAGEN6 [hp_X]
    FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA6 [hp_X]
    SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY) SUS SCROFA PANCREAS6 [hp_X]
    BOS TAURUS BONE (UNII: TRS31EO6ZN) (BOS TAURUS BONE - UNII:TRS31EO6ZN) BOS TAURUS BONE8 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-7016-21350 in 1 BOTTLE, GLASS; 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(48951-7016)
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