Label: AURUM OLIBANUM MYRRHA 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 February 25, 2026

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  • PURPOSE

    Uses: Temporary relief of environmental sensitivity and calms and relieves stress.

  • INDICATIONS & USAGE

    FOR ORAL USE ONLY

  • DOSAGE & ADMINISTRATION

    Directions: Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow. Follow inside instructions to open ampule.

  • WARNINGS

    Warnings:
    NOT FOR INJECTION
    Do not use if allergic to any ingredient. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use.
    Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • ACTIVE INGREDIENT

    Active Ingredients: Myrrha (Myrrh resin) 7X, Olibanum (Rubber resin from wood of incense tree) 7X, Aurum met. ( Metallic gold) 10X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt

    Prepared using rhythmical processes.

  • QUESTIONS

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

    Lot:

  • PRINCIPAL DISPLAY PANEL

    Aurum Olibanum Myrrha Ampule

  • INGREDIENTS AND APPEARANCE
    AURUM OLIBANUM MYRRHA 
    aurum olibanum myrrha liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1196
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MYRRH (UNII: JC71GJ1F3L) (MYRRH - UNII:JC71GJ1F3L) MYRRH7 [hp_X]  in 1 mL
    FRANKINCENSE (UNII: R9XLF1R1WM) (FRANKINCENSE - UNII:R9XLF1R1WM) FRANKINCENSE7 [hp_X]  in 1 mL
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD10 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-1196-110 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(48951-1196)
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