Bonscent Hand Sanitizer Basic
Product Images NDC 73981-010

2 FDA label images from Microbiome9 Life Science · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Bonscent Hand Sanitizer Basic (NDC 73981-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Microbiome9 Life Science, 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

Image Of Carton (100ea Carton)

Image Of Carton (100ea Carton)
Drug Facts panel for BONSCENT HAND SANITIZER BASIC GEL listing active ingredient as 62.0% alcohol and purpose as antiseptic. It includes uses for reducing bacteria on skin and repeated use, warnings about external use, flammability, eye contact, and ingestion, and directions for application and supervision of children under 6 years. Other information notes storage temperature, fabric discoloration, and potential harm to wood/plastics. Inactive ingredients list includes water, carbomer, triethanolamine, glycols, lavender oil, strawberry extract, and pomegranate extract. Distributor and manufacturer details and net weight of 3mL single-use packets are included.*
FDA Label Image

Image Of Carton (50ea Carton)

Image Of Carton (50ea Carton)
Drug Facts panel for BONSCENT HAND SANITIZER BASIC GEL by Microbiome9 Life Science. It lists active ingredient as 62% alcohol with antiseptic purpose. Includes uses, warnings, directions, other information, inactive ingredients, and distributor/manufacturer details. Net weight is 3mL x 50 single use packets. Also states it kills 99.99% of germs and is dermatologically tested.*

* 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.