Micox Solution/ Drops
Product Images NDC 17089-420

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Micox (NDC 17089-420). 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

5usmic Rev04 03 07 18

This is a description of a product manufactured by GUNA Sp.a. in Italy and distributed by GUNA Inc. in the United States. The product is a 30ml/1.0 fl. oz. liquid containing ethyl alcohol 30%. It provides temporary relief of symptoms related to fungal yeast overgrowth in skin and mucosa, such as skin rashes, redness, itching, intestinal gas, and bloating. The warning notes that if symptoms persist for more than 5 days, or if pregnant or breastfeeding, one should consult a doctor. The product has not been evaluated by the FDA.*

* 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.