Label: BAMBUSA VISCUM STANNUM 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 December 16, 2024

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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: Formica (Red wood ant) 5X, Bambusa (Bamboo) 6X, Betonica (Wood betony) 6X, Disci intervert. (Bovine intervertebral discs of the cervical, thoracic and lumbar spine) 6X, Rosmarinus (Rosemary) 6X, Viscum Mali (Apple tree mistletoe) 6X, Stannum met. (Metallic tin) 7X, Jasper (Semiprecious stone) 12X, Equisetum (Horsetail) 15X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt, Lactose

    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. 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 Lot:

  • PRINCIPAL DISPLAY PANEL

    Bambusa Viscum Stannum Ampules

  • INGREDIENTS AND APPEARANCE
    BAMBUSA VISCUM STANNUM 
    bambusa viscum stannum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2023
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FORMICA RUFA (UNII: 55H0W83JO5) (FORMICA RUFA - UNII:55H0W83JO5) FORMICA RUFA5 [hp_X]  in 1 mL
    BAMBUSA VULGARIS WHOLE (UNII: WCD45M1BSK) (BAMBUSA VULGARIS WHOLE - UNII:WCD45M1BSK) BAMBUSA VULGARIS WHOLE6 [hp_X]  in 1 mL
    STACHYS OFFICINALIS (UNII: UO9989Y17N) (STACHYS OFFICINALIS - UNII:UO9989Y17N) STACHYS OFFICINALIS6 [hp_X]  in 1 mL
    BOS TAURUS INTERVERTEBRAL DISC (UNII: 0A04Z76C13) (BOS TAURUS INTERVERTEBRAL DISC - UNII:0A04Z76C13) BOS TAURUS INTERVERTEBRAL DISC6 [hp_X]  in 1 mL
    ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) (ROSMARINUS OFFICINALIS FLOWERING TOP - UNII:8JM482TI79) ROSMARINUS OFFICINALIS FLOWERING TOP6 [hp_X]  in 1 mL
    VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP6 [hp_X]  in 1 mL
    TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN7 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE12 [hp_X]  in 1 mL
    EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP15 [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:48951-2023-110 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(48951-2023)