Durafast Hand Sanitizer
Product Images NDC 76795-750

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Durafast Hand Sanitizer (NDC 76795-750). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Printjet Corp, 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

76795-749- 01 60 mL (76795 749 01 60ml)

Drug Facts and label text for DuraFast Hand Sanitizer gel with 70% alcohol antiseptic. Includes purpose, usage instructions, warnings, inactive ingredients, storage information, and emergency contact details. Text is provided in both English and French. Details usage precautions, age restrictions, and safety advisories for external use only.*

FDA Label Image

76795-749-02 120 mL (76795 749 02 120ml)

DuraFast Hand Sanitizer 4 oz (120 mL) label, produced by PRINTJET CORP. The label indicates the product is an antiseptic alcohol-based gel sanitizer with lavender fragrance. It features Drug Facts and info in English and French, including active ingredient content around 70% alcohol. The label includes usage warnings, directions, and manufacturer details along with a barcode and FDA registration.*

FDA Label Image

76795-749-04 237 mL (76795 749 04 237ml)

Drug Facts panel for DuraFast Hand Sanitizer containing 70% alcohol as the active ingredient. It lists purpose as antiseptic, usage instructions for hand sanitization, warnings for external use, storage conditions, and directions for use. The panel includes precautions about keeping it out of children’s reach, avoiding contact with eyes, and storing below 40°C. The text is presented in both English and French.*

FDA Label Image

76795-749-05 475 mL (76795 749 05 475ml)

Drug Facts label for DuraFast Hand Sanitizer Gel with 70% alcohol antiseptic. The label includes usage instructions, warnings, directions, and storage information in English and French. It indicates a lavender fragrance, product volume of 16 oz (475 mL), and notes the product is a non-sterile topical solution made in the USA by PrintJet Corp and distributed by Sector Nine Distribution Ltd.*

FDA Label Image

76795-749-06 950 mL (76795 749 06 950ml)

DuraFast Hand Sanitizer Gel 70% Alcohol, 32 oz (950 mL) bottle label by PRINTJET CORP. The label highlights antiseptic alcohol hand sanitizer gel with lavender fragrance, a 70% topical solution, non-sterile. The front panel includes usage instructions, warnings, and storage information with bilingual English and French text. It features FDA registration and recycling logos.*

FDA Label Image

76795-749-07 3785 mL (76795 749 07 3785ml)

Drug Facts text panel for DuraFast Hand Sanitizer with 70% alcohol as the active ingredient. Includes antiseptic purpose, uses, warnings, directions, and inactive ingredients. The panel is bilingual in English and French, providing detailed safety and usage instructions. The label also highlights the product as a 1 gallon (3785 mL) topical, non-sterile hand sanitizer gel with lavender fragrance, made in the USA, and distributed by Sector Nine Distribution Ltd.*

FDA Label Image

76795-749-19 8550 mL (76795 749 19 8550ml)

Drug Facts panel of DuraFast Hand Sanitizer Gel showing the active ingredient as 70% Alcohol for antiseptic use. The label includes usage instructions, warnings, directions, storage, and inactive ingredients. It also features bilingual information in English and French, highlighting its lavender fragrance and non-sterile topical solution of 2.25 gallons (8550 mL) produced by PRINTJET CORP.*

* 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.