Nanobio Protect Nasal Antiseptic Solution
Product Images NDC 74315-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nanobio Protect Nasal Antiseptic Solution (NDC 74315-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluewillow Biologics, 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

Carton (Carton)

The packaging label of NanoBio Protect Nasal Antiseptic Solution with 0.13% benzalkonium chloride, an antiseptic. It highlights helping reduce the risk of infection, killing 99.99% of germs, and being alcohol-free and fragrance-free. The label notes moisturizing benefits and persistence on skin for over 4 hours. The package is for 0.61 FL OZ (18 mL) with 40 treatments, distributed by BlueWillow Biologics, Inc. Included is a Drug Facts panel with active ingredient, uses, warnings, directions, other information, inactive ingredients, and contact information.*

FDA Label Image

Greenbox

Packaging label for NanoBio Protect Nasal Antiseptic Solution by BlueWillow Biologics, Inc. The label highlights the active ingredient benzalkonium chloride (0.13%) as an antiseptic. It emphasizes ease of use with instructions to shake, dip, and swab, claims to kill 99.99% of germs, and states the product is alcohol-free, fragrance-free, moisturizing, and soothing. The bottle size is 0.61 FL OZ (18 mL), providing 40+ treatments. The label also includes drug facts, warnings, directions, inactive ingredients, and contact information.*

FDA Label Image

Whitebottle

Label of NanoBio Protect Nasal Antiseptic Solution containing benzalkonium chloride 0.13% as the active ingredient. The antiseptic solution is packaged in an 18 mL (0.61 fl oz) bottle and labeled by BlueWillow Biologics, Inc. The label includes the NDC 74315-001-01 and lists inactive ingredients such as edetate disodium, glycerin, poloxamer 407, refined soybean oil, sodium chloride, and water.*

* 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.