ARNICA
ARNICA is an FDA drug label for the active ingredient ARNICA MONTANA manufactured by Boiron administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230929.
Generic: ARNICA MONTANA
Manufacturer: Boiron
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 0220-9089
Application:
Effective: 20230929
Active Ingredients: Active ingredients** (in each tablet) Arnica montana 30X HPUS (2.5 mg) The letters HPUS indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.
Indications & Usage
Uses* temporarily relieves muscle pain and stiffness due to: minor injuries overexertion falls reduces symptoms of bruising such as: pain swelling discoloration
Dosage & Administration
Adults and children 6 years for age and older - At the onset of symptoms, dissolve 2 tablets in the mouth and repeat every hour for 2 more hours. Then, dissolve 2 tablets in the mouth every 6 hours until symptoms are relieved. Children 2 to 5 years of age: Dissolve 2 tablets in 1 tablespoon of water for easier intake. Follow directions above. Children under 2 years of age: Ask a doctor.
Contraindications
Not available.
Warnings
Not available.
Adverse Reactions
Not available.
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