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 Vitamedica Inc. 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.
Active Ingredient:
Arnica Montana 30X.
Purpose:
Anti-Inflammatory
Warnings:
If pregnant or breast-feeding ask a health professional before use. Discontinue use if any adverse reactions occur. Contact your physician, if symptoms do not subside within 14 days.
KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if seal is broken or shows any signs of tampering.
Keep Out Of Reach Of Children:
KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.
Directions:
Adults, three tablets, three times a day. Not intended for children under 12 years of age. This product is a sublingual application.
Uses:
Temporary relief of bruising, swelling and pain associated with soft tissue injury.
Inactive Ingredients:
Copovidone, Crospovidone, Lactose, Magnesium Stearate, Mannitol, Microcrystalline Cellulose, Silicon Dioxide, and Sorbitol.
Questions:
Formulated and Distributed
by VitaMedica Corp.
Torrance, CA 90502
888-367-8605 VitaMedica.com
©2021 VitaMedica Corporation
NDC 65111-005-66
Package Display Label
VitaMedica
Arnica Montana
30X HPUS
REDUCES
Bruising, Swelling & Pain
NATURAL REMEDY
STIMULATES HEALING
Recommended by Plastic Surgeons
Homeopathic Medicine
120 Sublingual Tablets
* Please review the disclaimer below.
