Durafast Hand Sanitizer
Product Images NDC 76795-749

7 FDA label images from Printjet Corp · 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 Durafast Hand Sanitizer (NDC 76795-749). 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

76795-749-11 60ml (76795 749 11 60ml)

76795-749-11 60ml (76795 749 11 60ml)
DuraFast Hand Sanitizer Spray packaging label by PRINTJET CORP. The label includes the product name with antiseptic alcohol active ingredient, presented in a 2 oz (60 mL) spray bottle. The label is bilingual (English and French) and highlights Lavender fragrance. It features dosing instructions, warnings, and a USP logo. The label displays drug facts, manufacturer information, and a barcode.*
FDA Label Image

76795-749-12 120ml (76795 749 12 120 mL)

76795-749-12 120ml (76795 749 12 120 mL)
DuraFast Hand Sanitizer Spray containing 75% alcohol with lavender fragrance, labeled as an antiseptic and topical solution. The 4 oz (120 mL) bottle label features usage directions, warnings, inactive ingredients, and regulatory symbols including the FDA logo. The label text is bilingual in English and French, provided by PRINTJET CORP.*
FDA Label Image

76795-749-14 237ml (76795 749 14 237ml)

76795-749-14 237ml (76795 749 14 237ml)
DuraFast Hand Sanitizer Spray label showing active ingredient alcohol 75% in an 8 oz (237 mL) spray bottle. The label highlights antiseptic use with lavender fragrance and states it is a 75% topical solution, non-sterile. The product is distributed by PRINTJET CORP, FDA registered, with usage directions, warnings, and storage instructions in English and French.*
FDA Label Image

76795-749-15 475 mL (76795 749 15 475ml)

76795-749-15 475 mL (76795 749 15 475ml)
DuraFast Hand Sanitizer Spray label by PRINTJET CORP featuring a 75% alcohol antiseptic topical solution with lavender fragrance. The front label states it is a 16 oz (475 mL) non-sterile spray that helps reduce bacteria. The label includes Drug Facts such as usage, warnings, directions, and active ingredient details.*
FDA Label Image

76795-749-16 950 mL (76795 749 16 950ml)

76795-749-16 950 mL (76795 749 16  950ml)
DuraFast Hand Sanitizer spray disinfectant label with 32 oz (950 mL) volume. Contains antiseptic alcohol with lavender fragrance. The label includes safety warnings, directions for use, and ingredient information. Manufactured by PrintJet Corp. The label features bilingual text in English and French.*
FDA Label Image

76795-749-17 3785 mL (76795 749 17 1 Gallon)

76795-749-17 3785 mL (76795 749 17 1 Gallon)
Label for DuraFast Hand Sanitizer Spray containing 75% antiseptic alcohol with lavender fragrance. The product is a 1-gallon (3785 mL) topical solution, non-sterile, and produced by PRINTJET CORP distributed by Sector Nine Distribution Ltd. The label is bilingual in English and French and includes warnings, directions, and contact information. The FDA registration number and a barcode are visible.*
FDA Label Image

76795-749-18 8550 mL (76795 749 18 8550 mL)

76795-749-18 8550 mL (76795 749 18 8550 mL)
DuraFast Hand Sanitizer Spray label featuring antiseptic with 75% alcohol as the active ingredient. The label highlights lavender fragrance and states the product is a 75% topical solution, non-sterile. The container size is 2.25 gallons (8550 mL). The label includes directions, warnings, and ingredient information in both English and French. It is labeled with the PRINTJET CORP as the distributor and contains FDA registration details and a barcode.*

* 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.