Home – Arnica Scorodite

Arnica Scorodite

FULL PRESCRIBING INFORMATION

Uses

Directions: FOR ORAL USE.

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

Active ingredient

Active Ingredients: Amethyst 6X, Arnica e pl. tota 6X, Conchae 6X, Levisticum e rad. 6X, Natrium carb. 6X, Orchis e tub. decoct. 6X, Apatite 7X, Scorodite 7X, Cerebellum 8X

Inactive Ingredients: Water, Salt, Lactose

Purpose

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Do not use if allergic to any ingredient. Consult a doctor before use if lactose intolerant. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Natural ingredients may cause color, scent and/or taste variation.

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

Arnica Scorodite

Arnica Scorodite LIQUID

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:48951-1155
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
COLLOIDAL SILICON DIOXIDE		6 [hp_X]
ARNICA MONTANA ARNICA MONTANA		6 [hp_X]
OSTREA EDULIS SHELL OSTREA EDULIS SHELL		6 [hp_X]
LEVISTICUM OFFICINALE ROOT LEVISTICUM OFFICINALE ROOT		6 [hp_X]
SODIUM CARBONATE		6 [hp_X]
ORCHIS MASCULA TUBER ORCHIS MASCULA TUBER		6 [hp_X]
FLUORAPATITE FLUORAPATITE		7 [hp_X]
FERROUS ARSENATE FERROUS ARSENATE		7 [hp_X]
BOS TAURUS CEREBELLUM BOS TAURUS CEREBELLUM		8 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
water
SODIUM CHLORIDE

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1		1 in 1 AMPULE
2	NDC:48951-1155-1	10 in 1 BOX

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
		2009-09-01

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!