Hand Sanitizer
Product Images NDC 76580-121

3 FDA label images from Bit Systems, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 76580-121). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bit Systems, Llc, 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

250g (250g 70hs Llrgel)

250g (250g 70hs Llrgel)
Drug Facts panel for Hand Sanitizer Gel by Bit Systems, LLC, featuring active ingredient Ethyl Alcohol 70% v/v as antiseptic. The gel is lemongrass and lavender scented with vitamin E and aloe vera. Includes warnings, directions for use, storage instructions, and inactive ingredients. Contact information and FDA NDC are also visible.*
FDA Label Image

4 Fl Oz (4o 70hs Lgrgel Fda)

4 Fl Oz (4o 70hs Lgrgel Fda)
Label for Hand Sanitizer Gel with Aloe Vera by Bit Systems, LLC. The label highlights active ingredient: 70% alcohol antiseptic. It features fragrances of lemongrass, lavender, and rosemary. Package size is 4 fluid ounces. The label includes usage instructions, warnings, and inactive ingredients listed in a text panel on the left. The product is made in America.*
FDA Label Image

8 Fl Oz (8o 70hs Lgrgel Fda)

8 Fl Oz (8o 70hs Lgrgel Fda)
The image shows the front and back label of SaneSanitizer Hand Sanitizer Gel with Aloe Vera, Lemongrass, Lavender, and Rosemary. It contains 70% alcohol antiseptic, comes in an 8 fl oz size, and is made by Bit Systems, LLC in America. The back label includes active ingredient information, warnings, directions, and contact details.*

* 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.