Joton Hand Sanitizer Gel
Product Images NDC 77078-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Joton Hand Sanitizer Gel (NDC 77078-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by L.q Joton Joint Stock Company- Paint Manufacturing Factory, 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

Bottle (Bottle)

Label for Joton Hand Sanitizer Gel alcohol 75% v/v, 500 ml, by L.Q Joton Joint Stock Company. The front shows the brand logo and product name with a claim to kill 99.9% of germs. The back includes a Drug Facts panel, usage instructions, warnings, inactive ingredients, manufacturer information, a barcode, and safety icons. The product is made in Vietnam.*

FDA Label Image

Bottle2 (Bottle2)

Label for Joton Hand Sanitizer Gel featuring the JOTON logo and highlighting 75% v/v alcohol content. The label includes a drug facts panel listing ethyl alcohol 75% v/v as the active antimicrobial ingredient. Directions, warnings, inactive ingredients, storage conditions, and manufacturer details for L.Q JOTON JOINT STOCK COMPANY are also present. The product net volume is 250 ml, and it is made in Vietnam.*

FDA Label Image

Bottle3 (Bottle3)

Joton Hand Sanitizer Gel packaging label shows a 100ml bottle containing 75% v/v alcohol. The label includes the Joton logo, antimicrobial claims, and detailed drug facts including active ingredient ethyl alcohol 75% v/v. Manufacturer is L.Q Joton Joint Stock Company- Paint Manufacturing Factory, Vietnam. Warnings, directions, and storage information are listed, along with barcodes 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.