Hand Sanitizer
Product Images NDC 74258-0009

3 FDA label images from New Holland Brewing Company, Llc · 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 Hand Sanitizer (NDC 74258-0009). 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)

Active Ingredient Section (Drug Facts Sp)
Drug Facts panel for Hand Sanitizer by New Holland Brewing Company, LLC, listing alcohol 80% v/v as the active ingredient for antiseptic purpose. The panel includes uses, warnings, directions, storage information, and inactive ingredients such as glycerin and hydrogen peroxide. Emphasizes external use only, flammability, and keeping out of reach of children.*
FDA Label Image

1 Gallon Principal Display (Sanitizer 1 Gal Nelbud)

1 Gallon Principal Display (Sanitizer 1 Gal Nelbud)
Label for Hand Sanitizer by New Holland Brewing Company, LLC, showing alcohol antiseptic 80% topical solution in a 1 gallon (3.78L) bottle. The label includes use directions, warnings, and ingredient information, with a barcode and NDC 74258-0009.*
FDA Label Image

8oz Principal Display (Sanitizer 8oz Nelbud)

8oz Principal Display (Sanitizer 8oz Nelbud)
Hand Sanitizer by New Holland Brewing Company, LLC. The label states it is an alcohol antiseptic 80% topical solution in an 8 fluid ounce (236 mL) bottle. The label includes Drug Facts with active ingredient alcohol 80% v/v, usage warnings, directions, storage information, and inactive ingredients. The product NDC is 74258-0009.*

* 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.