Arnica Scorodite by Uriel Pharmacy Inc. ARNICA SCORODITE pellet

Arnica Scorodite by

Drug Labeling and Warnings

Arnica Scorodite by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION

Dissolve pellets under the tongue 3-4
times daily. Ages 12 and older: 10 pellets.
Ages 2-11: 5 pellets. Under age 2: Consult
a doctor.

ACTIVE INGREDIENT

Active Ingredients: Amethyst (Nat. silicic acid anhydrate with traces of manganese and iron) 6X, Arnica 6X, Conchae (Oyster shells) 6X, Levisticum (Lovage) 6X, Natrium carb. (Sodium carbonate monohydrate) 6X, Orchis tub. decoct. (Orchid) 6X, Apatite (Nat. calcium fluorophosphate) 7X, Scorodite (Nat. ferric arsenate) 7X, Cerebellum (Bovine cerebellum) 8X

INACTIVE INGREDIENT

Inactive Ingredients: Sucrose, Lactose

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. 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. Do not use if safety seal is broken or missing.

QUESTIONS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARNICA SCORODITE 
arnica scorodite pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-1156
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6 [hp_X]
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	6 [hp_X]
OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (OSTREA EDULIS SHELL - UNII:49OY13BE7Z)	OSTREA EDULIS SHELL	6 [hp_X]
LEVISTICUM OFFICINALE ROOT (UNII: 46QZ19OEX8) (LEVISTICUM OFFICINALE ROOT - UNII:46QZ19OEX8)	LEVISTICUM OFFICINALE ROOT	6 [hp_X]
SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D)	SODIUM CARBONATE	6 [hp_X]
ORCHIS MASCULA TUBER (UNII: 5H2N55J61B) (ORCHIS MASCULA TUBER - UNII:5H2N55J61B)	ORCHIS MASCULA TUBER	6 [hp_X]
FLUORAPATITE (UNII: M4CM1H238J) (FLUORAPATITE - UNII:M4CM1H238J)	FLUORAPATITE	7 [hp_X]
FERROUS ARSENATE (UNII: 129CO35H12) (FERROUS ARSENATE - UNII:129CO35H12)	FERROUS ARSENATE	7 [hp_X]
BOS TAURUS CEREBELLUM (UNII: Q09851U44F) (BOS TAURUS CEREBELLUM - UNII:Q09851U44F)	BOS TAURUS CEREBELLUM	8 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
LACTOSE (UNII: J2B2A4N98G)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	3mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-1156-2	1350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	09/01/2009

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

Labeler - Uriel Pharmacy Inc. (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy Inc.		043471163	manufacture(48951-1156)