Hepar Sulphuris Calcareum Pellet
Product Images NDC 0220-2464

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 0220-2464). 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

2nd Panel

2nd Panel
A drug facts panel continuation showing inactive ingredients lactose and sucrose. It provides contact information for Boiron USA and instructions on how to dispense pellets from the bottle, illustrated in three steps: turn the tube upside down, twist until 5 pellets are dispensed, then remove the cap and use it to pour pellets under the tongue.*
FDA Label Image

3rd Panel

3rd Panel
Drug Facts panel for Hepar sulphuris calcareum pellets containing 0.443 mg of active ingredient per pellet. Includes sections on uses, warnings about stopping use and consulting a doctor if symptoms persist or if pregnant/breastfeeding, directions for dosing in adults and children, and a note about not using if the pellet dispenser seal is broken.*
FDA Label Image

Hepsulcal8x

Hepsulcal8x
Hepar sulphuris calcareum 8x oral pellet homeopathic medicine by Boiron, made in France. The label includes lot and expiration placeholders, a symptom indication for painful and hoarse dry cough worsened by cold weather, and a statement about approximately 80 pellets contained. The package includes a disclaimer that claims are based on homeopathic practice not evaluated by the FDA.*

* 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.