Apis Mellifica 200ck Pellet
Product Images NDC 76472-3002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Apis Mellifica 200ck (NDC 76472-3002). 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

Page3_label_ollois_common (Page3 Label Ollois Common)

A continuation panel of Drug Facts for APIS MELLIFICA 200CK sublingual pellets, listing organic sucrose as the inactive ingredient. The panel includes homeopathic dilution information (**C, K, CK & X), distributor contact details for SEVENE USA Inc., and pictorial instructions on how to dispense pellets from the tube by turning it upside down, twisting the cap, and placing pellets under the tongue. The bottom features branding and website information for Ollois.*

FDA Label Image

Label_ollois_apis_mellifica_200ck_page1 (Label Ollois Apis Mellifica 200ck Page1)

Packaging label for Apis Mellifica 200ck homeopathic medicine pellets by SEVENE USA. The label shows it is an organic, lactose-free, sublingual pellet product with approximately 80 pellets weighing 4 grams. The product is made in France and includes the barcode and NDC 76472-3002-1.*

FDA Label Image

Label_ollois_apis_mellifica_200ck_page2 (Label Ollois Apis Mellifica 200ck Page2)

Drug Facts panel for APIS MELLIFICA 200CK pellets shows active ingredient and usage for stinging edemas from stings or allergies. The panel includes warnings about use during pregnancy, overdoses, and keeping out of reach of children. Directions advise dissolving 5 pellets under the tongue three times daily. Other information covers storage and tamper-evidence instructions.*

* 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.