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

Arniflora

Nature's Way Products, Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Arniflora



FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient:

ARNICA MONTANA  1 X HPUS 8%

Inactive Ingredients:














Dosage and Administration:

Boericke and Tafel Brand:

Directions:



Uses


Indications and Usage:

For the temporary relief of bruises and minor muscle and joint pain, swelling and stiffness from over-exercising, sprains, falls, blows, and sports injuries.


Purpose

Purpose:

For the temporary relief of bruises and minor muscle and joint pain,
swelling and stiffness from over-exercising, sprains, falls, blows, and sports
injuries.


Warnings

Do not use on broken skin.  For external use only.  Avoid contact with eyes. Discontinue use of this product and consult a doctor if redness occurs or condition worsens or symptoms persist for more than 7 days or clear up and recur again within a few days. Keep out of reach of children.  In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.


Keep out of Reach of Children:

Keep out of reach of children.

Ask the Doctor:

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.


Package Label.Principal Display Panel:

























Arniflora

ARNICA MONTANA GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53499-5090
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARNICA MONTANA ARNICA MONTANA 1 [hp_X]

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
CARBOMER HOMOPOLYMER TYPE C
water
WITCH HAZEL
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 28 in 1 TUBE
2 78 in 1 TUBE
3 NDC:53499-5090-1 1 in 1 PACKET

Marketing Information

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


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.