Antibacterial Hand Sanitizer Gel
Product Images NDC 70412-135

2 FDA label images from Zhejiang Ayan Biotech Co.,ltd. · 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 Antibacterial Hand Sanitizer (NDC 70412-135). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zhejiang Ayan Biotech Co.,ltd., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Label10 (Label10)

Label10 (Label10)
Antibacterial Hand Sanitizer gel, 1 oz (30 mL) bottle label. The front shows the product name and net volume. The back label displays Drug Facts including the active ingredient Ethyl Alcohol 62% as antiseptic, uses for hand sanitizing, warnings for external use only and flammability, and directions for use. Additional information notes storage recommendations, inactive ingredients, distributor details, and country of manufacture (China).*
FDA Label Image

Label9 (Label9)

Label9 (Label9)
The image shows front and back panels of packaging for Antibacterial Hand Sanitizer gel. The front states the product name and net volume of 0.5 oz (15 mL). The back panels include Drug Facts listing Ethyl Alcohol 62% as the active ingredient, its use for hand sanitizing, warnings about flammability and external use, directions for application, and inactive ingredients. It also notes the product is made in China and includes storage instructions.*

* 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.