Gp Reeves Hand Sanitizer
Product Images NDC 74258-0010

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gp Reeves Hand Sanitizer (NDC 74258-0010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by New Holland Brewing Company, 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.

FDA Label Image

Active Ingredient Section (Drug Facts Sp)

Drug Facts panel for GP Reeves Hand Sanitizer, listing Alcohol 80% v/v as the active ingredient with antiseptic purpose. Includes usage instructions for hand sanitation, warnings about flammability and proper external use, precautions for children under 2 months and open wounds, directions for use, storage conditions, and inactive ingredients. A bold warning to keep out of reach of children is also shown.*

FDA Label Image

Principal Display Panel (Sanitizer 1 Gal Gpreeves)

The label for GP Reeves Hand Sanitizer is a 1 gallon (3.78L) non-sterile topical solution with 80% alcohol antiseptic. It features the brand name and product type prominently, instructions for use, warnings, and storage information. The label also states it is made by New Holland Brewing Company, LLC in Holland, MI, USA, and includes the product NDC 74258-0010 and a barcode.*

FDA Label Image

Sanitizer 32oz Gp Reeves

Label of GP Reeves Hand Sanitizer featuring 80% alcohol antiseptic topical solution in a 32 fl. oz. (946 mL) bottle. The label includes Drug Facts detailing active ingredient alcohol 80% v/v as antiseptic, usage directions, warnings, and inactive ingredients. It is manufactured by New Holland Brewing Company in Holland, MI, USA, and bears hazard icons for flammability and irritation.*

* 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.