Label: MANDRAGORA RHEUM 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 November 22, 2023

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  • INDICATIONS & USAGE

    Directions: FOR ORAL USE.

  • DOSAGE & ADMINISTRATION

    Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

  • ACTIVE INGREDIENT

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

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt, Lactose

  • 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. Do not use if allergic to any ingredient. 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.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    Mandragora Rheum Ampules

  • INGREDIENTS AND APPEARANCE
    MANDRAGORA RHEUM 
    mandragora rheum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-7015
    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]  in 1 mL
    TARAXACUM PALUSTRE ROOT (UNII: GCZ4W7077C) (TARAXACUM PALUSTRE ROOT - UNII:GCZ4W7077C) TARAXACUM PALUSTRE ROOT3 [hp_X]  in 1 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER6 [hp_X]  in 1 mL
    BOVINE TYPE I COLLAGEN (UNII: FHJ3ATL51C) (BOVINE TYPE I COLLAGEN - UNII:FHJ3ATL51C) BOVINE TYPE I COLLAGEN6 [hp_X]  in 1 mL
    FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA6 [hp_X]  in 1 mL
    SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY) SUS SCROFA PANCREAS6 [hp_X]  in 1 mL
    BOS TAURUS BONE (UNII: TRS31EO6ZN) (BOS TAURUS BONE - UNII:TRS31EO6ZN) BOS TAURUS BONE8 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-7015-110 in 1 BOX09/01/2009
    11 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package
    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(48951-7015)
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