Phytolacca Decandra Pellet
Product Images NDC 0220-4022

3 FDA label images from Boiron · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Phytolacca Decandra (NDC 0220-4022). 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

2nd Panel

2nd Panel
This image shows a Drug Facts panel continuation including inactive ingredients lactose and sucrose, with contact information for Boiron USA and instructions to see the website for homeopathic dilutions. It also features illustrated step-by-step instructions on how to dispense pellets from the product container, including turning the tube upside down, twisting until pellets are dispensed into the cap, and removing the cap to pour pellets under the tongue.*
FDA Label Image

3rd Panel

3rd Panel
Drug Facts panel for Phytolacca decandra pellets includes active ingredient information, usage guidance, warnings to stop use and consult a doctor if symptoms persist or if pregnant or breastfeeding, directions for adults and children to dissolve 5 pellets under the tongue 3 times daily, and a caution not to use if the pellet dispenser seal is broken.*
FDA Label Image

Phytodec6x

Phytodec6x
Label of Phytolacca decandra 6X oral pellets, a homeopathic medicine by Boiron made in France. The label includes the NDC number 0220-4022-41 and notes it contains approximately 80 pellets. It also states the product is for sore throat pain radiating to the ears and advises to peel for drug facts and instructions for use.*

* 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.