Clean Sept Alcohol Antiseptic 70% - Topical Hand Sanitizer Non-sterile Gel
Product Images NDC 79916-001

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Clean Sept Alcohol Antiseptic 70% - Topical Hand Sanitizer Non-sterile Gel (NDC 79916-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Be Factory Laboratories Industria Comercio Importacao E Exportacao Ltda, 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

Label Gel 1500 mL (Labelling Clean Sept Hand Sanitizer Gel 1.5 L Rev01)

Drug Facts panel for Clean Sept Alcohol Antiseptic 70% topical hand sanitizer gel lists active ingredient as 70% denatured ethyl alcohol, its use to reduce bacteria when soap and water aren't available, warnings about flammability and external use only, directions for application, storage instructions, and inactive ingredients. Manufacturer information for Be Factory Laboratories in Brazil is also included along with contact details for adverse event reporting.*

FDA Label Image

Label Gel 200 mL (Labelling Clean Sept Hand Sanitizer Gel 200 mL Rev01)

Drug Facts panel for Clean Sept Alcohol Antiseptic 70% - Topical Hand Sanitizer Non-Sterile Gel showing active ingredient as Denatured Ethyl Alcohol 70% v/v, purpose as antiseptic, uses, warnings, directions, other information, and inactive ingredients. The label includes storage instructions, manufacturer details, volume of 6.7 fl. oz. (200 ml), and a barcode. Product made in Brazil by Be Factory Laboratories Industria Comercio Importacao e Exportacao Ltda.*

FDA Label Image

Label Gel 3 mL (Labelling Clean Sept Hand Sanitizer Gel 3 mL Rev01)

Drug Facts text panel for Clean Sept Alcohol Antiseptic 70% Topical Hand Sanitizer Non-Sterile Gel describes active ingredient as Denatured Ethyl Alcohol 70%, purpose as antiseptic, and its use to reduce bacteria when soap and water are unavailable. It includes warnings, directions, storage information, inactive ingredients, and contact details for reporting adverse events. The volume is 0.1 fl. oz. / 3 ml.*

FDA Label Image

Label Gel 500 mL (Labelling Clean Sept Hand Sanitizer Gel 500 mL Rev01)

Drug Facts panel for Clean Sept Alcohol Antiseptic 70% Topical Hand Sanitizer Non-Sterile Gel 16.9 fl. oz. The panel includes active ingredient (Denatured Ethyl Alcohol 70%), uses, warnings, directions for use, other storage information, inactive ingredients, and contact information for adverse event reporting. Manufactured by Be Factory Laboratories in Brazil.*

FDA Label Image

Label Gel 5000 mL (Labelling Clean Sept Hand Sanitizer Gel 5l Rev01)

Drug Facts panel for Clean Sept Alcohol Antiseptic 70% - Topical Hand Sanitizer Non-Sterile Gel with denatured ethyl alcohol 70% v/v as active ingredient. It includes uses, warnings, directions, storage instructions, inactive ingredients, and contact information for reporting adverse events. The product is labeled as made in Brazil by Be Factory Laboratories Industria Comercio Importacao e Exportacao Ltda and comes in a 1.3 gal (5 L) container.*

* 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.