Hand Sanitizer
Product Images NDC 74988-732

8 FDA label images from Sanitizenow Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74988-732). 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

Tote (1041 L 75 V2)

Tote (1041 L 75 V2)
Drug Facts panel for Hand Sanitizer by SanitizeNow Inc., listing Ethyl Alcohol 75% as the active antiseptic ingredient. Includes usage directions, warnings, and storage information. The label emphasizes FDA registration, manufacturing in the USA, and features usage instructions with illustrated steps for hand sanitizing. The product comes in a 1041 L (275 Gal) container.*
FDA Label Image

4 Oz (118 mL 75 V2)

4 Oz (118 mL 75 V2)
This drug facts label for Hand Sanitizer by SanitizeNow Inc. lists the active ingredient as Ethyl Alcohol 75% with antiseptic purpose. It includes warnings, directions for use, storage information, and inactive ingredients. The label also features usage instructions with illustrations and states the product size as 118 mL (4 oz).*
FDA Label Image

Drum (208 L 75 V2)

Drum (208 L 75 V2)
Hand Sanitizer by SanitizeNow Inc., 75% Ethyl Alcohol antiseptic formula, in a 208 L (55 Gal) container. The label features the brand name Porrexx, instructions for use, drug facts including warnings and inactive ingredients, and states the product is FDA registered with NDC 74988-732-55.*
FDA Label Image

8 Oz (236 mL 75 V2)

8 Oz (236 mL 75 V2)
Drug Facts panel for Hand Sanitizer shows active ingredient Ethyl Alcohol 75% as an antiseptic. It includes usage directions, warnings, and inactive ingredients like water and glycerin. Instructions with images illustrate proper hand sanitizing steps. Label states product volume is 236 mL (8 oz), with information about FDA registration and NDC 74988-732-80, manufactured in the USA.*
FDA Label Image

Tanker (25741 L 75 V2)

Tanker (25741 L 75 V2)
Drug Facts panel for Hand Sanitizer by SanitizeNow Inc. The active ingredient is Ethyl Alcohol 75% as an antiseptic. It includes directions for use, warnings, and other information on storage and inactive ingredients. The label also features branding for 'Porrexx High Potency Hand Sanitizer' with 7% alcohol formula, plant extracts, and skin conditioner, FDA registration details, NDC 74988-732-74, and illustrated usage steps.*
FDA Label Image

1 Gal (3.79 L 75 V2)

1 Gal (3.79 L 75 V2)
Drug Facts panel for Hand Sanitizer by SanitizeNow Inc. listing Ethyl Alcohol 75% as the active ingredient with antiseptic purpose. Includes warnings, directions, storage information, and inactive ingredients. Features usage instructions with illustrations and states the product is made in the USA and FDA registered.*
FDA Label Image

16 Oz (473 mL V2)

16 Oz (473 mL V2)
The image is a drug facts and usage panel for Porrexx High Potency Hand Sanitizer by SanitizeNow Inc. It highlights 75% ethyl alcohol as the active ingredient and includes warnings, directions for use, and storage information. The panel also illustrates a step-by-step hand sanitizing process with four pictograms, plus FDA registration and product volume of 473 mL (16 oz).*
FDA Label Image

2 Oz (59 mL 75 V2)

2 Oz (59 mL 75 V2)
Drug Facts panel for Hand Sanitizer by SanitizeNow Inc. showing active ingredient Ethyl Alcohol 75% as antiseptic. Includes usage instructions, warnings, directions for use, storage info, and inactive ingredients. Adjacent instructions illustrate proper hand sanitizing steps in four icons. Volume listed as 59 mL (2 oz). The product is FDA registered with NDC 74988-732-20.*

* 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.