Arsenicum Sulphuratum Flavum Pellet
Product Images NDC 0220-0544

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 Arsenicum Sulphuratum Flavum (NDC 0220-0544). 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)
A Drug Facts panel continuation showing inactive ingredients lactose and sucrose. It provides contact information for questions or comments, including a phone number and website BoironUSA.com. Instructions on how to dispense pellets from the container are illustrated and described in three steps: turning the tube upside down, twisting until pellets are dispensed into the cap, then removing the cap and placing pellets under the tongue.*
FDA Label Image

Label (3rd Panel)

Label (3rd Panel)
Drug Facts panel for Arsenicum sulphuratum flavum pellets, detailing active ingredient amount per pellet, usage directions, warnings including to stop use and consult a doctor if symptoms persist or if pregnant or breastfeeding, and additional information about not using if the pellet dispenser seal is broken.*
FDA Label Image

Label (Arssulfla8x)

Label (Arssulfla8x)
Arsenicum sulphuratum flavum 8x homeopathic medicine pellets by Boiron, made in France. The label includes lot and expiration fields, states indication for dry cough aggravated by cold, and notes approximately 80 pellets per container. It is an oral pellet product of arsenic trisulfide for human OTC use.*

* 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.