Drosera Pellet
Product Images NDC 0220-1796

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Drosera (NDC 0220-1796). 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)

This panel continues the Drug Facts for Drosera 30 hp C pellets, listing inactive ingredients lactose and sucrose. It includes customer service contact information for Boiron USA. Directions with illustrations explain how to dispense pellets from the container: turn tube upside down, twist until 5 pellets are released into the cap, then carefully remove the cap and use it to place pellets under the tongue.*

FDA Label Image

Label (3rd Panel)

A Drug Facts panel providing information on the active ingredient amount per pellet, use instructions referencing the front panel, warnings about symptom duration and pregnancy, directions for adults and children on dosing frequency, and additional instructions about pellet dispenser seal integrity.*

FDA Label Image

Label (Drosera30c)

Drosera 30C oral pellets by Boiron, labeled as a homeopathic medicine made in France. The label notes an approximate count of 80 pellets per package. It includes usage instructions to peel for Drug Facts and instructions and mentions the lot and expiration date fields. The label states this product is for spasmotic dry cough worsened at night and by heat and clarifies that claims are based on traditional homeopathic practice, not accepted 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.