Berberis Vulgaris Pellet
Product Images NDC 0220-0841

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Berberis Vulgaris (NDC 0220-0841). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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FDA Label Image

Label (Bervul1m)

Label (Bervul1m)
Berberis vulgaris is a homeopathic medicine made in France. It contains approx. 80 pellets, and is used for skin rash with round, red patches and thin flakes. It should be dissolved under the tongue three times a day until symptoms are relieved or as directed by a doctor. The active ingredient is 0.443 mg per pellet. If symptoms persist for more than 3 days or worsen, stop using it, and consult a doctor. It should be kept out of reach of children, and not used if the pellet dispenser seal is broken. Inactive ingredients include lactose, sucrose. For more information, visit BoironUSA.com.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.