Indications & Usage
Directions: FOR ORAL USE.
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Arnica Betula B (NDC 48951-1384). 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.
Directions: FOR ORAL USE.
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
Active Ingredients: Betula e fol. (Silver birch leaves) 3X, Betula (cort.) dec. (Silver birch, bark dried) 4X, Cerebellum (Bovine cerebellum) 17X, Corpora quadrigemina (Bovine Quadrigeminal plate) 17X, Epiphysis (Bovine pineal body) 17X, Labyrinthus (Bovine inner ear) 17X, Medulla oblong. (ventr. quart.) (Bovine Myelencephalon ) 17X, Nervus statoacusticus (Bovine eighth cranial nerve) 17X, Arnica e pl. tota (Arnica) 30X, Onyx (Nat. Silicic acid with traces of iron oxide and carbon) 30X, Plumbum mellitum (Lead with honey) 30X, Formica ex animale 30X
Inactive Ingredients: Water, Salt
Prepared using rhythmical processes.
Use: Temporary relief of headache.
KEEP OUT OF REACH OF CHILDREN.
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. 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.
Questions? Call 866.642.2858 Made by Uriel, East Troy, WI 53120 shopuriel.com Lot:
* Please review the disclaimer below.