Nux Vomica Pellet
Product Images NDC 76472-3027

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nux Vomica (NDC 76472-3027). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sevene Usa, 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

Page 3 (Page3 Label Ollois Common)

Drug Facts panel (continued) from NUX VOMICA 200ck pellet label showing inactive ingredient as organic sucrose. Instructions for dispensing pellets include turning the dispensing tube upside down, twisting the cap to dispense pellets, and using the cap to place pellets under the tongue. Distributed by SEVENE USA Inc. with contact details for questions or comments, and website information for ollois.com.*

FDA Label Image

Page 1 (Label Ollois Nux Vomica 200ck Page1)

Label for Nux Vomica 200ck homeopathic medicine by SEVENE USA. The label states it contains approximately 80 pellets weighing 4 grams total, with the route of administration as sublingual pellets. The product is organic, lactose-free, made in France, and labeled with NDC 76472-3027-1. It is traditionally used for indigestion and nausea associated with overindulgence, with a disclaimer about traditional homeopathic claims.*

FDA Label Image

Page 2 (Label Ollois Nux Vomica 200ck Page2)

Drug Facts panel for NUX VOMICA 200CK pellets, sublingual dosage form. It lists the active ingredient as Nux Vomica 200CK, uses for indigestion and nausea associated with overindulgence, warnings including to stop use and consult a doctor if symptoms persist, and directions to dissolve 5 pellets under the tongue three times daily. Additional information covers storage instructions and tamper-evidence seal caution.*

* 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.