Guna-dermo Solution/ Drops
Product Images NDC 17089-295

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Guna-dermo (NDC 17089-295). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guna Spa, 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

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The packaging label for GUNA-DERMO homeopathic medicine solution/drops, manufactured by Guna spa. The label shows the product name prominently, lists it as a 30 ml (1.0 fl. oz.) oral solution containing 30% ethyl alcohol. The label provides detailed drug facts including active ingredients such as Arsenicum album 6C, Belladonna 6C, Dulcamara 6C, Echinacea angustifolia 6C, Graphites 6C, Interleukin 1 beta 7C, Interleukin 2 4C, Melatonin 4C, Plantago major 4C, and Sulfur 6C and their purposes. Directions for use, warnings, storage information, and company contact details are also included.*

* 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.