Proteus Pellet
Product Images NDC 0220-4163

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 Proteus (NDC 0220-4163). 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.

Product Images & Figures Index

FDA Label Image

2nd Panel

2nd Panel
This panel provides additional drug facts including inactive ingredients lactose and sucrose. It offers contact information for questions, including a phone number and website. Instructions for dispensing pellets are illustrated in three steps: turning the tube upside down, twisting until five pellets are dispensed, and removing the cap to pour pellets under the tongue.*
FDA Label Image

3rd Panel

3rd Panel
Drug Facts panel for Proteus pellets including active ingredient amount (0.443 mg per pellet), general instructions to see symptoms and product name on the front panel, warnings about usage duration and pregnancy, directions for administering 5 pellets under the tongue three times daily, and advice not to use if the pellet dispenser seal is broken.*
FDA Label Image

Proteus8x

Proteus8x
Packaging label for Proteus 8X homeopathic medicine pellets by Boiron, labeled as a human prescription drug with NDC 0220-4163-41. The label notes the medicine is made in France, includes approximately 80 pellets, and is for oral use. It states the product is RX only and contains a notice about being based on traditional homeopathic practice not recognized by medical evidence.*

* 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.