Aconitum Napellus Pellet
Product Images NDC 76472-3000

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Aconitum Napellus (NDC 76472-3000). 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)

Page 3 (Page3 Label Ollois Common)
The image shows a Drug Facts continuation panel for ACONITUM NAPELLUS 200ck pellets with Organic Sucrose listed as the inactive ingredient. It explains that C, K, CK, and X indicate homeopathic dilutions and provides contact information for SEVENE USA Inc. It includes illustrated instructions on dispensing pellets from a tube and a website link to ollois.com.*
FDA Label Image

Page 1 (Label Ollois Aconitum 200ck Page1)

Page 1 (Label Ollois Aconitum 200ck Page1)
The label for ACONITUM NAPELLUS 200ck homeopathic pellets by SEVENE USA features a green and peach design. It states the product is organic and lactose-free, traditionally used to temporarily reduce sudden fever and cough associated with cold or flu. The package contains approximately 80 pellets weighing 4 grams and is made in France. The label includes a barcode and the NDC 76472-3000-1.*
FDA Label Image

Page 2 (Label Ollois Aconitum 200ck Page2)

Page 2 (Label Ollois Aconitum 200ck Page2)
Drug Facts panel for ACONITUM NAPELLUS 200CK pellets. It lists the active ingredient as Aconitum Napellus 200CK, uses for reducing sudden fever and cough from cold or flu, warnings including consulting a doctor if symptoms persist or if pregnant, directions to dissolve 5 pellets under the tongue three times a day, and additional storage and safety information.*

* 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.