Berberis vulgaris
Berberis vulgaris is an FDA drug label for the active ingredient BERBERIS VULGARIS ROOT BARK 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 20231109.
Generic: BERBERIS VULGARIS ROOT BARK
Manufacturer: Boiron
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 0220-0835
Application:
Effective: 20231109
Active Ingredients: Berberis vulgaris 4X (**contains 0.443 mg of the active ingredient per pellet)
Indications & Usage
Skin rash with round, red patches and thin flakes*
Dosage & Administration
Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
Contraindications
Not available.
Warnings
Not available.
Adverse Reactions
Not available.
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