MEDULLA ARNICA- medulla arnica liquid
Uriel Pharmacy Inc.

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.

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Medulla Arnica

Directions: FOR ORAL USE.

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

Active Ingredients: Cornu cervi (Stag’s horn) 8X, Medulla spin. (Bovine spinal cord) 8X, Stibium met. (Antimony) 8X, Aurum met. (Metallic gold) 10X, Betula (Silver birch bark) 10X, Jasper (Semiprecious stone) 17X, Arnica 20X

Inactive Ingredients: Water, Salt

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 Uriel, East Troy, WI 53120 www.urielpharmacy.com

MedullaArnicaAmpules

MEDULLA ARNICA
medulla arnica liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-7021
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CERVUS ELAPHUS WHOLE (UNII: AE45O9AR61) (CERVUS ELAPHUS WHOLE - UNII:AE45O9AR61)	CERVUS ELAPHUS WHOLE	8 [hp_X] in 1 mL
BOS TAURUS SPINAL CORD (UNII: 03Z3I85RNE) (BOS TAURUS SPINAL CORD - UNII:03Z3I85RNE)	BOS TAURUS SPINAL CORD	8 [hp_X] in 1 mL
ANTIMONY (UNII: 9IT35J3UV3) (ANTIMONY - UNII:9IT35J3UV3)	ANTIMONY	8 [hp_X] in 1 mL
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	10 [hp_X] in 1 mL
BETULA PUBESCENS BARK (UNII: 3R504894L9) (BETULA PUBESCENS BARK - UNII:3R504894L9)	BETULA PUBESCENS BARK	10 [hp_X] in 1 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	17 [hp_X] in 1 mL
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	20 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-7021-1	10 in 1 BOX	09/01/2009	07/07/2022
1		1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009	07/07/2022

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-7021)

Revised: 7/2022

Document Id: e33c6585-d77f-0547-e053-2a95a90ad493

Set id: 9fea58e1-77cf-4169-9bda-ea58764f9c0e

Version: 4

Effective Time: 20220707

Uriel Pharmacy Inc.