Aconitum Napellus
Aconitum Napellus is an FDA drug label for the active ingredient ACONITUM NAPELLUS manufactured by OHM PHARMA 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 20211229.
- Generic name
- ACONITUM NAPELLUS
- Manufacturer
- OHM PHARMA INC.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 66096-777
- Application
- N/A
- Label effective
- 20211229
Active ingredients
Indications & Usage
USE: To be used according to standard homeopathic indications.
Dosage & Administration
DIRECTIONS: Dissolve 3-5 pellets under the tongue 3 times a day or as directed by a professional.
Contraindications
Not available.
Warnings
WARNINGS: Keep out of reach of children. If pregnant or breast-feeding, ask a health care professional before use. Stop use and ask a health care professional if symptoms persist for more than 3 days or worsen. Keep out of reach of children.
Adverse Reactions
Not available.