Drosera Pellet
Product Images NDC 0220-1792

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 Drosera (NDC 0220-1792). 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)

Label (2nd Panel)
Continuation of the Drug Facts panel for Drosera 12 [hp_C] pellet oral homeopathic drug by Boiron. Lists inactive ingredients lactose and sucrose, contact information for questions, and distributor details. Includes instructions with illustrations on how to dispense pellets by turning the tube upside down, twisting until 5 pellets fall into the cap, then removing the cap to pour pellets under the tongue.*
FDA Label Image

Label (3rd Panel)

Label (3rd Panel)
Drug Facts panel for Drosera pellets, listing the active ingredient Drosera Rotundifolia at 12 hp_C strength with 0.443 mg per pellet. It includes warnings to stop use and consult a doctor if symptoms persist, directions for dosing five pellets under the tongue three times daily, and other information about pellet dispenser seal safety.*
FDA Label Image

Label (Drosera12c)

Label (Drosera12c)
Drosera 12C oral pellets by Boiron, a homeopathic medicine made in France. The label includes a lot and expiration date section, a statement indicating the product is for spasmotic dry cough worsened at night and by heat, and notes the package contains approximately 80 pellets. A peel-off section directs users to drug facts and usage 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.