Drosera Pellet
Product Images NDC 0220-1793

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Drosera (NDC 0220-1793). 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

Label (2nd Panel)

A Drug Facts panel continuation listing inactive ingredients lactose and sucrose, with contact information for BoironUSA including email and phone number. It provides instructions for using Boiron homeopathic dilutions and details distribution by Boiron Inc., Newtown Square, PA. Illustrations show how to dispense pellets: turning the tube upside down, twisting to dispense five pellets into the cap, then removing the cap to place pellets under the tongue.*

FDA Label Image

Label (3rd Panel)

Drug Facts panel detailing active ingredient information, uses, warnings, directions, and other information for an oral pellet product. It notes the active ingredient amount per pellet, usage instructions for adults and children, warnings about symptom duration and pregnancy or breastfeeding, and a caution about using the product if the pellet dispenser seal is broken.*

FDA Label Image

Label (Drosera15c)

Label for Drosera 15c pellets, an oral homeopathic medicine by Boiron, made in France. The label includes the HPUS NDC 0220-1793-41 and states the indication for spasmodic dry cough worsened at night and by heat. It notes approximately 80 pellets are contained and directs to peel for drug facts and instructions.*

* 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.