GNC BIO-REMEDY ARNICA RELIEF- arnica montana tablet

GNC BIO-REMEDY ARNICA RELIEF by

Drug Labeling and Warnings

GNC BIO-REMEDY ARNICA RELIEF by is a Homeopathic medication manufactured, distributed, or labeled by Homeocare Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients:

Arnica Montana 30C (HPUS)

Inactive Ingredients:

Lactose, Magnesium Stearate.

Purpose:

Provides homeopathic relief for pain, bruising, muscle aches, injuries and pre-and-post surgical support.

Keep out of reach of children.

Keep out of reach of children.

Indications & Usage:

Temporarily relieves the pain and stiffness of injuries, sprains and muscle aches due to injuries.

Warnings:

If you are pregnant or breastfeeding, seek the advice of a healthcare professional before using this product.

pain persists for more than 3 days or if pain, redness or swelling worsens, or new symptoms occur, consult a healthcare professional because these could be signs of a serious condition. Keep this and all medicines put of the reach of children. Do not use if cap seal if broken or missing.

Dosage and Administration:

Chew one tablet and allow to dissolve in the mouth. Take one tablet every 30 minutes until symptoms improve, then reduce to every 4 hours or as needed. For adult use only.

GNC Bio Remedy Arnica Relief Tablets

image of gnc arnica relief tablets

INGREDIENTS AND APPEARANCE

GNC BIO-REMEDY ARNICA RELIEF 
arnica montana tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61727-801
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	30 [hp_C]

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

Product Characteristics
Color	white	Score	2 pieces
Shape	ROUND	Size	10mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61727-801-00	100 in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/30/2012

Labeler - Homeocare Laboratories (088248828)