Instant Hand Sanitizer Spray
Product Images NDC 76402-422

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Instant Hand Sanitizer (NDC 76402-422). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hillyard Gmp, 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-01 (Image 01)

Image-01 (Image 01)
The packaging label for Hillyard Instant Hand Sanitizer Spray features the product name prominently with instructions for cartridge installation and removal depicted in small diagrams. It includes contact information for Hillyard Industries, Inc., a barcode, and indicates net contents of 33.8 fluid ounces or 1 liter. The label's design emphasizes the Affinity dispensing system with purple and white colors.*
FDA Label Image

Image-02 (Image 02)

Image-02 (Image 02)
Label for Hillyard Instant Hand Sanitizer spray, topical use, with branding for the Affinity Dispensing System. The label includes instructions for placing and removing the cartridge from the dispenser, barcode, manufacturer contact information, and net contents stated as 33.8 fluid ounces or 1 liter.*
FDA Label Image

Image 03

Image 03
Packaging label for Instant Hand Sanitizer Spray by Hillyard GMP. The label features the product name prominently, with 62% ethyl alcohol indicated as the active ingredient. It states the net contents as 1 liter (0.264 gallon) and highlights moisturizing ingredients such as aloe, vitamin E, and conditioners. The label background includes blue and white colors with a green aloe leaf image.*

* 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.