Aurum Olibanum Myrrha Liquid
FDA Label NDC 48951-1196

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Aurum Olibanum Myrrha (NDC 48951-1196). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Indications & Usage

Directions: FOR ORAL USE.

Dosage & Administration

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

Otc - 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

Otc - Purpose

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

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Warnings

Warnings: 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.

Otc - Questions

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

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