Home – Arnica Montana

Arnica Montana

FULL PRESCRIBING INFORMATION

Arnica montana 6C

anti-inflammatory

Temporarily relieves

Do not use if you have an allergy or hypersensitivity to the components of the formula.

Stop use and ask a doctor if:

condition worsens
if symptoms persist for more than 7 days or clear up and occur again within a few days
rash develops

If pregnant or breast feeding, consult a health professional.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

Store in a cool and dry place

Sucrose

Questions or comments? information@nartexlabs.com or call 1-800-838-0916 between 9am and 5pm CST

Arnica Montana

Arnica Montana PELLET

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:34666-091
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA ARNICA MONTANA		6 [hp_C]

Inactive Ingredients
Ingredient Name	Strength
SUCROSE

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:34666-091-50	150 in 1 BOTTLE, GLASS

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
		2011-07-01

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!