Phosphorus Pellet
Product Images NDC 76472-3028

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Phosphorus (NDC 76472-3028). 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)

This drug facts panel continuation lists the inactive ingredient as Organic Sucrose and explains homeopathic dilution symbols C, K, CK, and X. It provides contact info for SEVENE USA, Pacoima, CA, and a toll-free number. Illustrated instructions explain how to dispense pellets by turning the tube upside down, twisting the cap, and placing pellets under the tongue. The bottom includes a promotional phrase and the brand name Olloïs.*

FDA Label Image

Page 1 (Label Ollois Phosphorus 200ck Page1)

Label for Phosphorus 200ck sublingual pellets by SEVENE USA, a homeopathic medicine. The label notes the product is organic, lactose-free, contains approximately 80 pellets (4g), and is made in France. It includes traditional uses such as relief of dry cough, bleeding, and dizziness, with a disclaimer about homeopathic claims. The NDC number 76472-3028 is shown along with branding for Ollo'is Homeopathy.*

FDA Label Image

Page 2 (Label Ollois Phosphorus 200ck Page2)

Drug Facts panel for Phosphorus 200CK indicating the active ingredient Phosphorus 200CK, uses for temporary relief of dry cough, bleeding, and dizziness, warnings including consulting a doctor if symptoms worsen, directions to dissolve 5 pellets under the tongue three times daily, and storage instructions to keep at room temperature along with tamper-evidence and organic verification details.*

* 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.