Defense Ag Disinfectant
Product Images NDC 79930-7116

3 FDA label images from Nexderma · 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 Defense Ag Disinfectant (NDC 79930-7116). 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

Ea 16 Oz H2o2 (Ea 16oz H202)

Ea 16 Oz H2o2 (Ea 16oz H202)
The Defense AG Sanitizing Disinfectant Spray label by Nexderma displays key ingredients including 80% Ethyl Alcohol, 0.12% Hydrogen Peroxide, and 10ppm Nano Silver Ag. The 16oz (473mL) spray claims to kill more than 99.99% of germs. The label includes usage instructions, warnings, manufacturer contact information, and the product NDC 79930-7116-4. Made in USA and recycling symbols are shown.*
FDA Label Image

Ea 1gal H2o2 (Ea 1gal H202)

Ea 1gal H2o2 (Ea 1gal H202)
Defense AG Disinfectant label by Nexderma, featuring 80% Ethyl Alcohol, 0.12% Hydrogen Peroxide, and 10ppm Nano Silver Ag as key ingredients. The label includes product name, disinfectant type, alcohol and peroxide content, package size of 1 gallon (3.79 L), usage warnings, ingredients, manufacturer address, barcode, and logos for Made in USA and recycling.*
FDA Label Image

Ea 32 Oz H2o2 (Ea 32oz H202)

Ea 32 Oz H2o2 (Ea 32oz H202)
Label of Defense AG Disinfectant Spray by Nexderma showing active ingredients 80% ethyl alcohol, 0.12% hydrogen peroxide, and 10 ppm nano silver Ag. The product volume is 32 oz (946 mL). The label includes uses, warnings, manufacturer contact details, and a barcode. It highlights killing 99.99% of germs.*

* 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.