Problend E3 Foaming Hand Sanitizer
Product Images NDC 76250-120

6 FDA label images from Seatex, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Problend E3 Foaming Hand Sanitizer (NDC 76250-120). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Seatex, 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

Pb0027120 E3 Foaming Hand Sanitizer 1.25 L Front Label

Pb0027120 E3 Foaming Hand Sanitizer 1.25 L Front Label
Label for Problend E3 Foaming Hand Sanitizer by Seatex, LLC, showing the product name and description as an all-in-one foaming hand sanitizer and cleanser, dye and fragrance free. The net contents are 1.25 liters (42 ounces). The label features an image of a hand dispensing foam from a pump bottle.*
FDA Label Image

Pb0027120 E3 Foaming Hand Sanitizer 1.25 L Labels 02

Pb0027120 E3 Foaming Hand Sanitizer 1.25 L Labels 02
The image shows the Drug Facts panel for Problend E3 Foaming Hand Sanitizer by Seatex, LLC. It lists Benzalkonium Chloride 0.1% as the active antimicrobial ingredient. The panel includes uses for hand sanitizing, warnings for external use with eye contact precautions, directions for use as foam, and inactive ingredients. Contact information and a barcode are present at the bottom.*
FDA Label Image

1 Gl Label (Pb0027120 E3 Foaming Hand Sanitizer 1 Gal Es Label)

1 Gl Label (Pb0027120 E3 Foaming Hand Sanitizer 1 Gal Es Label)
Label for Problend E3 Foaming Hand Sanitizer, a 1 gallon (3.785 L) foaming hand sanitizer and cleanser containing Benzalkonium Chloride 0.1% as the active ingredient. The label is bilingual in English and Spanish, displaying usage, warnings, directions, and inactive ingredients. Manufactured by Seatex, LLC with safety classifications and a barcode.*
FDA Label Image

55 Gl Label (Pb0027120ac E3 Foaming Hand Sanitizer 55 Gal Es Label)

55 Gl Label (Pb0027120ac E3 Foaming Hand Sanitizer 55 Gal Es Label)
Label for Problend E3 Foaming Hand Sanitizer by Seatex, LLC, showing usage instructions, active ingredient Benzalkonium Chloride 0.1%, and package size 55 gallons/208 liters. The label includes bilingual English and Spanish text, safety warnings, and a photograph of a hand dispensing foam sanitizer.*
FDA Label Image

275 Gl Label (Pb0027120ad E3 Foaming Hand Sanitizer 275 Gal Es Label)

275 Gl Label (Pb0027120ad E3 Foaming Hand Sanitizer 275 Gal Es Label)
Label for Problend E3 Foaming Hand Sanitizer by Seatex, LLC, showing the product name and usage as an all-in-one foaming hand sanitizer and cleanser. The label includes bilingual (English and Spanish) drug facts with active ingredient Benzalkonium Chloride 0.1%, and net contents of 275 gallons (1041 liters). The label also displays hazard classification icons, manufacturer contact info, and a photograph of a person dispensing foam from a pump bottle.*
FDA Label Image

330 Gl Label (Pb0027120ae E3 Foaming Hand Sanitizer 330 Gal Es Label)

330 Gl Label (Pb0027120ae E3 Foaming Hand Sanitizer 330 Gal Es Label)
Problend E3 Foaming Hand Sanitizer label from Seatex, LLC displaying the product name, a hand dispensing foam image, active ingredient Benzalkonium Chloride 0.1%, drug facts, and instructions in both English and Spanish. The label indicates a large container size of 330 gallons (1249 L) and includes safety warnings, inactive ingredients, and an emergency contact number. The label also shows health, flammability, and physical hazard classifications with all rated zero and a Made in USA flag.*

* 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.