Drosera Pellet
Product Images NDC 0220-1784

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 0220-1784). 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)
This image shows part of a Drug Facts panel for Drosera pellets by Boiron, listing inactive ingredients lactose and sucrose. It includes a customer service contact and distributor address, with instructions on how to dispense pellets from the container: turning the tube upside down, twisting to release 5 pellets, and carefully removing the cap to pour pellets under the tongue.*
FDA Label Image

Label (3rd Panel)

Label (3rd Panel)
Drug Facts panel containing active ingredient information (amount per pellet), usage instructions, warnings about symptom duration and pregnancy, directions for administration under the tongue, and a caution regarding the pellet dispenser seal. Text is in blue on a white background.*
FDA Label Image

Label (Drosera5c)

Label (Drosera5c)
Drosera 5C oral pellets homeopathic medicine by Boiron, made in France. The label shows the product name, strength (5C), lot and expiration fields, and indication for spasmoc dry cough worsened by night and heat. It contains approximately 80 pellets and includes instructions to peel for drug facts and usage directions. The label notes the product is not evaluated by FDA and is based on traditional homeopathic practice.*

* 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.