Hand Sanitizer
Product Images NDC 74988-730

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74988-730). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sanitizenow Inc., 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

Updated Purrexx Label 1041 L (275 Gal) 80 V2

Drug Facts panel of Hand Sanitizer by SanitizeNow Inc. listing active ingredient as Alcohol 80% with antiseptic purpose. Includes usage instructions, warnings, directions for use, and storage information. Additional label text highlights the FDA registration, product quantity of 1041 L (275 gallons), and four-step hand sanitizing instructions with simple illustrations.*

FDA Label Image

Updated Purrexx Label 16 Oz (473 mL) 80 V2

Drug Facts panel for Hand Sanitizer by SanitizeNow Inc. showing active ingredient alcohol 80% as antiseptic. Includes uses for reducing bacteria when soap and water unavailable, warnings against use in children under 2 months and on open wounds, directions for application, and storage information. Additional instructions illustrate dispensing, rubbing hands palm to palm, rubbing fingertips, and drying hands thoroughly. Label states FDA registration and 473 mL (16 oz) volume.*

FDA Label Image

Updated Purrexx Label 2 Oz (59 mL) 80 V2

Drug Facts panel for Hand Sanitizer by SanitizeNow Inc. shows 80% alcohol as the active ingredient and lists its antiseptic purpose. It includes uses, warnings, directions for use, and inactive ingredients such as water and glycerin. The text advises on storage conditions and cautions about avoiding use on children under 2 months and open wounds. It also displays steps for proper hand sanitizing and states the product is FDA registered with NDC 74988-730-20.*

FDA Label Image

Updated Purrexx Label 208 L (55 Gal) 80 V2

Label for Hand Sanitizer by SanitizeNow Inc., featuring the brand name Porrexx and indicating a high potency formula with 80% alcohol. The label states the product is made with plant extracts and skin conditioner, with a volume of 208 liters (55 gallons). It includes Drug Facts with active ingredient, uses, warnings, directions, inactive ingredients, and FDA registration details. The label also shows step-by-step hand sanitizing instructions and a barcode.*

FDA Label Image

Updated Purrexx Label 25741 L (6800 Gal) 80 V2

Drug Facts panel for Hand Sanitizer with 80% alcohol as active ingredient. Includes use instructions, warnings, directions, and inactive ingredients. The label emphasizes FDA registration, manufacturing in the USA, and displays directions with icons illustrating proper hand sanitizing steps. The product is named Parrexx, noting high potency and plant extracts included, with a volume of 25741 L (6800 Gal).*

FDA Label Image

Updated Purrexx Label 3.79 L (1 Gal) 80 V2

Drug Facts panel for Hand Sanitizer by SanitizeNow Inc. showing active ingredient Alcohol 80% as antiseptic, directions for use, warnings including flammability, and inactive ingredients. Additional labeling highlights high potency 80% alcohol formula, plant extracts, skin conditioner, FDA registration, product volume 3.79L (1 Gal), usage instructions, and barcode.*

FDA Label Image

Updated Purrexx Label 4 Oz (118 mL) 80 V2

Drug Facts panel for Hand Sanitizer by SanitizeNow Inc. showing active ingredient Alcohol 80% as an antiseptic, use instructions, warnings, directions for use, and inactive ingredients. Also includes usage illustrations for applying the hand sanitizer, FDA registration info, and product branding with claims of high potency and plant extracts. The product size is 4 oz (118 mL).*

FDA Label Image

Updated Purrexx Label 8oz (236ml) 80 V2

The label for Porrexx High Potency Hand Sanitizer by SanitizeNow Inc. displays 80% alcohol formula, made with plant extracts and skin conditioner. The 8 oz (236 mL) container label includes usage instructions, warnings, and inactive ingredients. The label features step-by-step hand sanitizing illustrations and FDA registration with NDC 74988-730-80.*

* 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.