Hydrastis Canadensis Pellet
Product Images NDC 0220-2522

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hydrastis Canadensis (NDC 0220-2522). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Boiron, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Hydcan6x

This is a description of a homeopathic medicine called Hydrastis Canadensis. The medicine comes in pellet form and is made in France. It is used for post-nasal drip and contains 0.443mg of the active ingredient per pellet. The medicine is to be taken by allowing 5 pellets to dissolve under the tongue three times a day. The inactive ingredients are lactose and sucrose. The medicine should not be used if the pellet dispenser seal is broken. In case of persistent symptoms lasting more than 3 days, a doctor should be consulted. If pregnant or breastfeeding, a healthcare professional should be consulted. Contact information for Boiron Inc., the company that distributes this medicine, is provided.*

FDA Label Image

Hydrastis Canadensis 6x Label

Hydrastis canadensis is a homeopathic medicine made in France and distributed by Boiron Inc. It contains less than 10 mg hydrastine, berberine alkaloids per pellet and is used for post-nasal drip. The active ingredient is 0.443 mg per pellet and it is taken by dissolving 5 pellets under the tongue 3 times a day until symptoms improve or as directed by a doctor. The medicine should not be used if the pellet dispenser seal is broken, and if symptoms persist or worsen, a doctor should be consulted. The medicine may not be suitable for pregnant or breastfeeding women without seeking advice from a healthcare professional.*

* 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.