Arnica Montana
Arnica Montana is an FDA drug label for the active ingredient ARNICA MONTANA manufactured by Schwabe North America, Inc. administered by SUBLINGUAL. 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 20220520.
Generic: ARNICA MONTANA
Manufacturer: Schwabe North America, Inc.
Product Type: HUMAN OTC DRUG
Route: SUBLINGUAL
Dosage Form:
NDC: 53499-3571
Application:
Effective: 20220520
Active Ingredients: Active Ingredient Arnica Montana 30C Inactive Ingredients CELLULOSE LACTOSE MONOHYDRATE MAGNESIUM STEARATE SODIUM CROSCARMELLOSE
Indications & Usage
Indications and Usage Temporarily relieves minor muscle or joint aches and pains from strains, sprains, bruises, backache, over extertion.
Dosage & Administration
Dosage and Administration Adults or children over 2 years: Take 3 tablets 1 to 3 times per day. Allow to dissolve under tongue. Indications and Usage Temporarily relieves minor muscle or joint aches and pains from strains, sprains, bruises, backache, over extertion. Purpose For the temporary relief of minor muscle or joint aches and pains from strains, sprains, bruises, backache and over exertion.
Contraindications
Not available.
Warnings
Warnings Do not use this product for pain for more than 10 days (adult) or 5 days (children) unless directed by a doctor.
Adverse Reactions
Not available.
More from same ingredient
365 Everyday Value Arnica
WFM Private Label, LP
ARNICA
STANDARD HOMEOPATHIC COMPANY
ARNICA
Boiron
ARNICA MONTANA
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
ARNICA MONTANA 200C
Natural Creations, Inc.
ARNICA MONTANA 30C
Natural Creations, Inc.
Arnica
BioActive Nutritional, Inc.
Arnica
Energique, Inc.