Capsicum Annuum Pellet
Product Images NDC 0220-1142

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 Capsicum Annuum (NDC 0220-1142). 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

Label (2nd Panel)

Label (2nd Panel)
A Drug Facts panel excerpt for Capsicum annuum oral pellets showing inactive ingredients lactose and sucrose, contact information for BoironUSA, and homeopathic dilutors details. Includes a three-step illustrated guide on how to dispense pellets: turn the tube upside down, twist to dispense 5 pellets into the cap, then remove the cap and use it to pour pellets under the tongue.*
FDA Label Image

Label (3rd Panel)

Label (3rd Panel)
Drug Facts panel for Capsicum annuum oral pellets, listing active ingredient amount per pellet, usage guidance, warnings including consultation for symptoms lasting more than 3 days or if pregnant or breastfeeding, directions for use including dosage frequency, and other information about pellet dispenser seal integrity.*
FDA Label Image

Label (Capann200ck)

Label (Capann200ck)
The label for Capsicum annuum 200 CK oral pellets, a homeopathic medicine by Boiron, made in France. It includes the NDC code 0220-1142-41, indicates approximately 80 pellets per package, and includes a lot and expiration date section. The label states it is not accepted medical evidence by FDA and advises 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.