Hand Sanitizer
Product Images NDC 74226-002

2 FDA label images from Homeland Energy Solutions, 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 Hand Sanitizer (NDC 74226-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Homeland Energy Solutions, 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

Denatured Alcohol Label 1200l (Denatured Alcohol Label 1200l)

Denatured Alcohol Label 1200l (Denatured Alcohol Label 1200l)
A text panel titled 'Denatured Alcohol' describing ethanol content of greater than 94.9% as determined by GC ASTM D5501. It specifies a quantity of 1200 liters and states the use is for producing hand sanitizer (antiseptic hand rubs) only. The product is labeled non-potable and provides manufacturer information for Homeland Energy Solutions, LLC, including address, phone number, email, FDA registration number (DUNS), and placeholders for manufacture and release dates and batch number.*
FDA Label Image

Denatured Alcohol Label 37850l (Denatured Alcohol Label 37850l)

Denatured Alcohol Label 37850l (Denatured Alcohol Label 37850l)
Text panel titled 'DENATURED Alcohol' describing ethanol with over 94.9% purity determined by GC ASTM D5501. States the quantity as 37,850 liters and notes it is for production use of hand sanitizer only, non-potable. Provides manufacturer details for Homeland Energy Solutions, LLC including address, phone, email, and FDA registration number. Mentions manufacturing and release dates and batch number fields, though these are blank.*

* 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.