Hygienex Hand Sanitizer
Product Images NDC 74588-790

7 FDA label images from Global Impact Innovation Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hygienex Hand Sanitizer (NDC 74588-790). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Global Impact Innovation 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

Hgxeucgel1glabel (Hgxeucgel1g)

Hgxeucgel1glabel (Hgxeucgel1g)
Hygienex Hand Sanitizer Eucalyptus Refreshing Gel label featuring a 1-gallon (3.78 L) refill container. The label highlights 72% alcohol antiseptic content, absence of synthetic fragrances, parabens, triclosan, and benzalkonium chloride. It includes directions for use, warnings, and inactive ingredients. Manufactured by Global Impact Innovation LLC, the label also features hand-washing illustrations and the NDC 74588-790-04.*
FDA Label Image

Hgxeucgel275glabel (Hgxeucgel275g)

Hgxeucgel275glabel (Hgxeucgel275g)
Drug Facts panel for Hygienex Eucalyptus Hand Sanitizer Gel topical solution with 72% alcohol antiseptic. It lists the active ingredient, uses, warnings, directions, and storage instructions. The label includes hazard warnings with safety precautions and disposal instructions, volume of 275 gallons, manufacturer information (Global Impact Innovation LLC), and batch details including lot number and manufacture date.*
FDA Label Image

Hgxeucgel32ozlabel (Hgxeucgel32oz)

Hgxeucgel32ozlabel (Hgxeucgel32oz)
Packaging label for Hygienex Hand Sanitizer Eucalyptus Refreshing Gel by Global Impact Innovation LLC. The label highlights it contains plant-derived alcohol, is free from synthetic fragrances, parabens, triclosan, and benzalkonium chloride. The product volume is 32 FL OZ (946 mL). The back label includes Drug Facts, warnings, directions for use, and ingredients, with contact information for the manufacturer in Galva, Illinois.*
FDA Label Image

Hgxeucgel330glabel (Hgxeucgel330g)

Hgxeucgel330glabel (Hgxeucgel330g)
Drug Facts panel for Hygienex Eucalyptus Hand Sanitizer by Global Impact Innovation LLC. It lists active ingredient as Alcohol 72% v/v with antiseptic purpose. Includes usage directions, warnings, precautions, and first aid instructions. Volume is 330 gallons with manufacturing date 07/2020. Hazard symbols for flammability and health risks are shown, along with safety and disposal guidelines.*
FDA Label Image

Hgxeucgel55glabel (Hgxeucgel55g)

Hgxeucgel55glabel (Hgxeucgel55g)
Drug Facts panel for Hygienex Eucalyptus Hand Sanitizer with 72% alcohol antiseptic gel topical solution. Includes active ingredient, usage warnings, directions, storage instructions, and safety precautions such as flammability warnings, prevention, and first aid measures from manufacturer Global Impact Innovation LLC.*
FDA Label Image

Hgxeucgel5glabel (Hgxeucgel5g)

Hgxeucgel5glabel (Hgxeucgel5g)
Drug Facts panel for Hygienex Eucalyptus Hand Sanitizer, showing active ingredient alcohol 72% as antiseptic. Includes warnings about flammability and usage restrictions, directions for use, inactive ingredients, and storage instructions. Also features safety hazard symbols, prevention measures, first aid instructions, and disposal guidance for the 5-gallon product from Global Impact Innovation LLC.*
FDA Label Image

Hgxeucgel64oz

Hgxeucgel64oz
Hygienex Hand Sanitizer Eucalyptus Refreshing Gel label by Global Impact Innovation LLC. The front label features the product name, eucalyptus scent, plant-derived alcohol, and absence of synthetic fragrances, parabens, triclosan, and benzalkonium chloride. The volume is 64 FL OZ (1.89 L). The back label displays drug facts including active ingredient ethyl alcohol 72%, usage warnings, directions, and manufacturer information with the NDC 74588-790.*

* 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.