ARNICA MONTANA 200C
ARNICA MONTANA 200C is an FDA drug label for the active ingredient ARNICA MONTANA manufactured by Natural Creations, Inc. 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 20220217.
Generic: ARNICA MONTANA
Manufacturer: Natural Creations, Inc.
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 43406-0311
Application:
Effective: 20220217
Active Ingredients: ACTIVE INGREDIENT (HPUS*): Arnica Montana 200C
Indications & Usage
USES: Temporarily relieves aches & pains from bruising & sore muscles.**
Dosage & Administration
DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.
Contraindications
Not available.
Warnings
WARNINGS: Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. KEEP OUT OF HTE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT Seal is broken or missing.
Adverse Reactions
Not available.
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