Antiseptic Hand Sanitizing Gel
Product Images NDC 79700-000

3 FDA label images from Jennychem Limited · 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 Antiseptic Hand Sanitizing Gel (NDC 79700-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Jennychem Limited, 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 (Label)

Label (Label)
Drug Facts panel for Antiseptic Hand Sanitizing Gel with 70% ethyl alcohol, listing active ingredient, purpose, uses, warnings, directions, inactive ingredients, and contact information. The panel advises external use only, flammability precautions, proper application instructions, and storage conditions by Jennychem Limited.*
FDA Label Image

Label2 (Label2)

Label2 (Label2)
Drug Facts panel for Antiseptic Hand Sanitizing Gel by Jennychem Limited, showing active ingredient as 70% ethyl alcohol with antiseptic purpose. Includes uses for hand washing to decrease bacteria, warnings for external use and flammability, directions for use, inactive ingredients, manufacturer details, and safety instructions.*
FDA Label Image

Label3 (Label3)

Label3 (Label3)
Label for Antiseptic Hand Sanitizing Gel 70% Ethyl Alcohol by Jennychem Limited. The front of the label features the product name, concentration, and volume of 1.3 gallons (5 liters). The back label includes Drug Facts with active ingredient ethyl alcohol 70%, uses, warnings, directions, inactive ingredients, manufacturer information, and safety warnings including flammability symbols.*

* 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.