ARNICA- arnica montana pellet

ARNICA by

Drug Labeling and Warnings

ARNICA by is a Homeopathic medication manufactured, distributed, or labeled by SEVENE USA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

HOMEOPATHIC DILUTION OF HPUS ARNICA MONTANA 30X.

PURPOSE

TRADITIONALLY USED FOR: PAIN FROM TRAUMA - BRUISES - STIFFNESS - MUSCLE SORENESS.

USE:

CONDITION LISTED ABOVE OR AS DIRECTED BY A PHYSICIAN.

DIRECTIONS:

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

WARNINGS:

Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

PREGNANCY OR 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.

OTHER INFORMATION:

Store at room temperature.

DO NOT USE

Do not use if pellet-dispenser seal is broken.

INACTIVE INGREDIENTS:

Sucrose.

QUESTIONS?

www.ollois.com * info@ollois.com* Made in Canada. Not reviewed by the FDA and not guaranteed to be effective.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARNICA 
arnica montana pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76472-1130
Route of Administration	SUBLINGUAL

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

Inactive Ingredients
Ingredient Name	Strength
sucrose (UNII: C151H8M554)

Product Characteristics
Color	white	Score
Shape	ROUND	Size	4mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76472-1130-1	80 in 1 CYLINDER; Type 0: Not a Combination Product	11/30/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/30/2011

Labeler - HBC NATURALS INC (969332936)