Gvr D-1106 Hand Sanitizer
Product Images NDC 77750-001

2 FDA label images from Grand Valley Reagents, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Gvr D-1106 Hand Sanitizer (NDC 77750-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Grand Valley Reagents, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Drug Facts (Gvr Drug Facts)

Drug Facts (Gvr Drug Facts)
Drug Facts panel for GVR D-1106 Hand Sanitizer by Grand Valley Reagents, LLC. It includes the active ingredient (Alcohol 80% v/v) listed as an antiseptic, use instructions, warnings about flammability, age restrictions, and safety precautions with eye contact and ingestion. Directions advise covering all surfaces of hands and supervising children under 6. Additional storage information and inactive ingredients (glycerin, hydrogen peroxide, purified water USP) are also included.*
FDA Label Image

Main Label (Gvr Hand Sanitizer Label 55gal)

Main Label (Gvr Hand Sanitizer Label 55gal)
Label for GVR D-1106 Hand Sanitizer by Grand Valley Reagents, LLC displays the company logo and contact information. It features hazard symbols indicating flammability and health risks, with warnings such as 'Highly flammable liquid and vapor' and 'Harmful if swallowed.' The label includes precautionary and first aid statements, an NFPA diamond with ratings, and specifies net contents as 55 gallons (208.2L). It also lists the product as alcohols, N.O.S., 3, PGIII with CAS numbers for several ingredients.*

* 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.