Nurinse Hand Sanitizer
Product Images NDC 77368-070

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nurinse Hand Sanitizer (NDC 77368-070). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nugentec, 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

Image (7736 807008)

NuRinse Hand Sanitizer label showing a 236 mL bottle size. The product contains 70% ethanol alcohol as the active ingredient. It is described as a personal care hand sanitizer with an advanced formula that moisturizes and meets WHO hand rub formulation guidelines. Labeler is NuGenTec, with contact details and a barcode included on the label.*

FDA Label Image

Image (77368 07010)

NuRinse Hand Sanitizer label showing a 1-gallon (approximately 3.8 L) container. It highlights personal care hand sanitizer with 70% ethanol as the active ingredient and mentions advanced moisturizing formula suitable for hospital and institutional use. The product is manufactured and distributed by NuGenTec, Emeryville, CA. The label includes directions, warnings, a barcode, and a QR code.*

FDA Label Image

Image (77368 07012)

Label of NuRinse Hand Sanitizer, a personal care hand sanitizer by NuGenTec. It features 70% ethanol alcohol as the active ingredient and includes moisturizing glycerin and hydrogen peroxide as inactive ingredients. The label highlights the World Health Organization recommended hand rub formulation, advanced moisturizing formula, and hospital/institutional grade quality for a 355 mL (12 FL OZ) bottle. Manufacturer contact and usage warnings are included.*

FDA Label Image

Image (77368 07016)

NuRinse Hand Sanitizer 473 mL label by NuGenTec features text highlighting it as a personal care hand sanitizer with 70% ethanol alcohol as the active ingredient. The label mentions the World Health Organization recommended hand rub formulation, moisturizing properties, and suitability for hospital and institutional use. Directions, warnings, manufacturer contact details, and a barcode are also displayed.*

* 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.