Arnica Montana description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Arnica Montana

Nature's Way Holding Co

Arnica Montana 6X




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient:
Arnica montana 6X



Inactive Ingredients:

CELLULOSE, MICROCRYSTALLINE

LACTOSE

MAGNESIUM STEARATE

CROSCARMELLOSE SODIUM









Dosage:

              Adults or children over 2 years. 

              Take 3 tablets 4-6 times a day. 

              Allow to dissolve under tongue. 

              Stop when symptoms are relieved.

Uses

Indications: For the temporary relief of minor muscle or joint aches and pain; strains, sprains, bruises, backache or over-exertion.  Characteristics: Pain, stiffness or swelling may be associated with acute injuries or trauma.

Purpose

Purpose: For the temporary relief of minor muscle or joint aches and pain; strains, sprains, bruises, backache or over-exertion. 

Warning: Do not take this product for pain for more than 10 days (adult) or 5 days (children) unless directed by a doctor. 

If pain persists or gets worse,  if new symptoms occur, or if redness or swelling is present, consult a doctor because these could be signs of a serious condition.

Pregnancy and Breast Feeding: If pregnant or breast-feeding, ask a health professional before use.

Keep Out of Reach of Children:  Keep out of reach of children.

Overdosage: In case of overdose, seek medical help or contact a Poison Control Center immediately.

Arnica Montana

Arnica Montana

Arnica Montana TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53499-3533
Route of Administration SUBLINGUAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARNICA MONTANA ARNICA MONTANA 6 [hp_X]

Inactive Ingredients

Ingredient Name Strength
cellulose, microcrystalline
LACTOSE
MAGNESIUM STEARATE
CROSCARMELLOSE SODIUM

Product Characteristics

Color Size Imprint Code Shape
white (white tablet) 6 mm B;T ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:53499-3533-2 100 in 1 BOTTLE, GLASS
2 NDC:53499-3533-3 250 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2006-01-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.