Label: BAMBUSA RHUS 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 13, 2024

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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: Gelsemium (Yellow jasmine) 4X, Gnaphalium (Edelweiss) 4X, Aconitum (Monkshood) 6X, Bambusa (Bamboo) 6X, Betonica (Wood betony) 6X, Mandragora (Mandrake) 6X, Rhus tox. (Sumac) 6X, Rosmarinus (Rosemary) 6X, Formica (Red wood ant) 7X, Disci intervert. (Bovine intervertebral discs of the cerv. thor. and lumbar spine) 8X, Granite (Primitive rock containing quartz, feldspar and mica) 10X, Jasper (Semiprecious stone) 12X, Argentum (SIlver) 20X, Arnica 20X

  • INACTIVE INGREDIENT

    Inactive Ingredient: Sucrose

    Prepared using rhythmical processes.

  • PURPOSE

    Use: Temporary relief of headache.

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

  • PRINCIPAL DISPLAY PANEL

    Bambusa Rhus Pellets

  • INGREDIENTS AND APPEARANCE
    BAMBUSA RHUS 
    bambusa rhus pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2017
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT4 [hp_X]
    PSEUDOGNAPHALIUM LUTEOALBUM LEAF (UNII: BGI20Z6M57) (PSEUDOGNAPHALIUM LUTEOALBUM LEAF - UNII:BGI20Z6M57) PSEUDOGNAPHALIUM LUTEOALBUM LEAF4 [hp_X]
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS6 [hp_X]
    BAMBUSA VULGARIS WHOLE (UNII: WCD45M1BSK) (BAMBUSA VULGARIS WHOLE - UNII:WCD45M1BSK) BAMBUSA VULGARIS WHOLE6 [hp_X]
    STACHYS OFFICINALIS (UNII: UO9989Y17N) (STACHYS OFFICINALIS - UNII:UO9989Y17N) STACHYS OFFICINALIS6 [hp_X]
    MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB) MANDRAGORA OFFICINARUM ROOT6 [hp_X]
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF6 [hp_X]
    ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) (ROSMARINUS OFFICINALIS FLOWERING TOP - UNII:8JM482TI79) ROSMARINUS OFFICINALIS FLOWERING TOP6 [hp_X]
    FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA7 [hp_X]
    BOS TAURUS INTERVERTEBRAL DISC (UNII: 0A04Z76C13) (BOS TAURUS INTERVERTEBRAL DISC - UNII:0A04Z76C13) BOS TAURUS INTERVERTEBRAL DISC8 [hp_X]
    PENOXSULAM (UNII: 784ELC1SCZ) (PENOXSULAM - UNII:784ELC1SCZ) PENOXSULAM10 [hp_X]
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE12 [hp_X]
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER20 [hp_X]
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA20 [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:48951-2017-21350 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(48951-2017)
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