Lathyrus Sativus Pellet
Product Images NDC 0220-3061

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 Lathyrus Sativus (NDC 0220-3061). 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

2nd Panel

2nd Panel
This image shows a portion of the Drug Facts panel for Lathyrus sativus pellets. It lists inactive ingredients lactose and sucrose, provides contact information for Boiron USA including phone and email, and gives a website for homeopathic dilutions. The panel also includes instructions in text and illustrations on how to dispense pellets: turning the tube upside down, twisting to dispense pellets into the cap, then removing the cap to pour the pellets under the tongue.*
FDA Label Image

3rd Panel

3rd Panel
Drug Facts panel describing the active ingredient quantity, usage warnings, directions for adults and children to take 5 pellets under the tongue three times daily at symptom onset, and other information including a caution against use if the pellet dispenser seal is broken. It refers to the front panel for active ingredient details and symptoms for use.*
FDA Label Image

Latsat30c

Latsat30c
Lathyrus sativus 30C homeopathic pellets packaging label showing the product as a homeopathic medicine by Boiron, made in France. The label notes the indication for muscular tiredness in the legs and includes instructions to peel for drug facts and usage. Approximately 80 pellets are contained in the package.*

* 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.