Every Man Jack - Hand Sanitizer
Product Images NDC 57934-5015

View Photos of 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 Every Man Jack - Hand Sanitizer (NDC 57934-5015). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Every Man Jack, 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

01b Lbl_emj_hand Sanitizer Spray_citrus_40ml (01b Lbl Emj Hand Sanitizer Spray 40ml)

01b Lbl_emj_hand Sanitizer Spray_citrus_40ml (01b Lbl Emj Hand Sanitizer Spray 40ml)
EVERY MAN JACK Hand Sanitizer Citrus 40 mL spray bottle packaging. Front features brand name, product type, scent, and effectiveness claim (99.9% effective against common germs). Back includes drug facts with active ingredient Ethanol 62%, usage, warnings, directions, inactive ingredients, and certifications for cruelty-free, gluten-free, vegan, and recyclability. Manufactured in the USA by EVERY MAN JACK.*
FDA Label Image

01b Lbl_emj_hand Sanitizer Spray_sea Salt_40ml (01b Lbl Emj Hand Sanitizer Spray Sea Salt 40ml)

01b Lbl_emj_hand Sanitizer Spray_sea Salt_40ml (01b Lbl Emj Hand Sanitizer Spray Sea Salt 40ml)
EVERY MAN JACK Hand Sanitizer Sea Salt label shows a 1.4 oz (40 mL) spray bottle product with 99.9% effectiveness against most common germs. The active ingredient is 62% Ethanol. The label includes warnings for flammability and external use, usage directions, inactive ingredients, and certifications such as cruelty-free, gluten-free, vegan, and recyclable. The product is made in the USA by EVERY MAN JACK.*

* 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.