Sanguinarinum Nitricum Pellet
Product Images NDC 0220-4554

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sanguinarinum Nitricum (NDC 0220-4554). 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 (Sanguinarinum Nitricum5c Label)

Sanguinarinum nitricum 5c homeopathic medicine pellets by Boiron in a rectangular label displaying product name, strength, made in France, active ingredient amount per pellet, lot and expiration identifiers, and approximate pellet count (80). The label includes a caution about pellet dispenser seal and a note to peel for drug facts and instructions for use.*

FDA Label Image

Label (Sanguinarinum Nitricum 5c Label)

Sanguinarinum nitricum 5c homeopathic medicine pellets by Boiron, made in France. The label states the product contains approximately 80 pellets with less than 10⁻⁵ mg sanguinarine per pellet. It includes directions for usage, warnings, inactive ingredients (lactose, sucrose), and instructions for dispensing pellets from the tube. Contact information for Boiron USA is provided.*

FDA Label Image

Label (Sannit5c)

Label for Sanguinarinum nitricum 5 c pellets, a homeopathic oral OTC drug by Boiron. The label states the product contains approximately 80 pellets and is made in France. It lists watery, burning nasal discharge during the day as a symptom on the front panel. Directions include dissolving 5 pellets under the tongue three times daily. Inactive ingredients are lactose and sucrose. Instructions show how to dispense pellets from the tube.*

* 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.