Hepar Sulphuris Calcareum Pellet
Product Images NDC 0220-2408

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 Hepar Sulphuris Calcareum (NDC 0220-2408). 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 a portion of the Drug Facts panel for Hepar sulphuris calcareum pellets, detailing inactive ingredients (lactose, sucrose), contact information for Boiron USA, and instructions on how to dispense pellets. The step-by-step guide illustrates turning the tube upside down, twisting to release 5 pellets into the cap, and carefully removing the cap to place pellets under the tongue.*
FDA Label Image

Label (3rd Panel)

Label (3rd Panel)
Drug Facts text panel for Hepar sulphuris calcareum pellets, providing information on the active ingredient amount per pellet, usage guidance, warnings including consulting a doctor if symptoms persist or if pregnant or breastfeeding, dosing directions for adults and children, and additional caution about pellet dispenser seal integrity.*
FDA Label Image

Label (Hepsulcal30x)

Label (Hepsulcal30x)
Label for Hepar sulphuris calcareum 30X oral pellets by Boiron, a homeopathic medicine made in France. The label notes it contains approximately 80 pellets. It includes space for lot and expiration dates and states use for painful and hoarse dry cough worsened by cold weather. Marked as US product NDC 0220-2408-41.*

* 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.