Arnica Montana Tablet
Product Images NDC 80004-200

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Arnica Montana (NDC 80004-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vitamedica, Inc., 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

150 Count Bottle Carton (Arnica 200c 150 Count Bottle Carton)

Packaging label for Arnica Montana 200C HPUS tablets by VitaMedica. The label features a blue and white color scheme and includes product branding, strength (200C HPUS), and quantity (150 tablets). It notes the product as a natural homeopathic remedy intended for oral use. The label also highlights the relief of pain, bruising, and swelling, with additional promotional terms like restoration, revitalization, and rejuvenation. A Drug Facts panel and a barcode are present on the packaging.*

FDA Label Image

150 Count Bottle (Arnica 200c 150 Count Bottle Label)

The image shows the packaging label for Arnica Montana 200C HPUS tablets by VitaMedica, Inc. The label is blue and white, indicating the product's maximum potency with 150 tablets in the package. The label lists the product as a homeopathic medicine that reduces pain, bruising, and swelling.*

FDA Label Image

30 Count Blister (Arnica 200c 30 Count Blister Carton)

The packaging label for Arnica Montana 200C HPUS tablets by VitaMedica, Inc. shows a blue and white design. The front panel highlights Arnica Montana 200C HPUS with maximum potency, stating it reduces pain, bruising, and swelling. It contains 30 quick-dissolving tablets in a 5-day blister pack. The side panel includes Drug Facts listing Arnica Montana 200C HPUS as the active ingredient, usage directions, warnings, and inactive ingredients. The label also mentions it is a homeopathic medicine for oral use, with the NDC 80004-200.*

* 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.