FDA Label for Arnica Montana
View Indications, Usage & Precautions
Arnica Montana Product Label
The following document was submitted to the FDA by the labeler of this product Schwabe North America. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredient:
Arnica montana 6X
Inactive Ingredient
Inactive Ingredients:
CELLULOSE, MICROCRYSTALLINE
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
CROSCARMELLOSE SODIUM
Dosage & Administration
Dosage:
Adults or children over 2 years: Take 3 tablets 4-6 times a day.
Allow to dissolve under tongue.
Indications & Usage
Indications:
Temporarily relieves minor muscle or joint aches and pain; strains, sprains, bruises, backache or over-exertion.
Otc - Purpose
Purpose: For the temporary relief of minor muscle or joint aches and pain; strains, sprains, bruises, backache or over-exertion.
Warnings
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.
Otc - Pregnancy Or Breast Feeding
Pregnancy and Breast Feeding: If pregnant or breast-feeding, ask a health professional before use.
Otc - Keep Out Of Reach Of Children
Keep Out of Reach of Children: Keep out of reach of children.
Overdosage
Overdosage: In case of overdose, seek medical help or contact a Poison Control Center immediately.
Boericke And Tafel Arnica Montana 6X 250T
Arnica-montana 6X_21103534_04
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