Defense Ag Disinfectant
Product Images NDC 79930-7109

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Defense Ag Disinfectant (NDC 79930-7109). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nexderma, 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

16oz Ea Disinfectant Label (Ndc Ea 16oz Hp Disinfectant)

Label for Defense AG Disinfectant Sanitizing Disinfectant Spray by Nexderma, featuring ingredients including 80% ethyl alcohol, 0.12% hydrogen peroxide, and 10 ppm nano silver Ag. The label indicates a 16 oz (473 mL) bottle and highlights germ-killing efficacy of 99.99%. Manufacturer contact information, usage instructions, warnings, and expiration data are also present on the label.*

FDA Label Image

1gal Ea Disinfectant Label (Ndc Ea 1gal Hp Disinfectant)

Label for Defense AG Disinfectant by Nexderma shows it as a sanitizing disinfectant containing 80% ethyl alcohol, 0.12% hydrogen peroxide, and 10 ppm nano silver Ag. The packaging states it kills 99.99% of germs and comes in a 1-gallon (3.79 L) container. The label includes ingredient, usage, and warning information, with manufacturer contact details and a barcode.*

FDA Label Image

32oz Ea Disinfectant Label (Ndc Ea 32oz Hp Disinfectant)

Label for Defense AG Disinfectant by Nexderma, a sanitizing disinfectant spray containing 80% Ethyl Alcohol, 1.2% Hydrogen Peroxide, and 10 ppm Nano Silver Ag. The label shows product volume as 32 oz (946 mL) with a statement of killing more than 99.99% of germs. Includes usage, warnings, inactive ingredients, lot number, expiration date, NDC 79930-7109-6, barcode, and maker information with contact details.*

* 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.