Zapro Hand Sanitizer
Product Images NDC 75209-011

View Photos of 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 Zapro Hand Sanitizer (NDC 75209-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guangdong Mingliu Technology Dail-use Chemical 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.

FDA Label Image

75209-011-01 250ml (75209 011 01 250ml)

75209-011-01 250ml (75209 011 01 250ml)
The image shows the Drug Facts panel for ZAPRO HAND SANITIZER by CAO Group, Inc. It lists Ethyl Alcohol 94% as the active antiseptic ingredient, usage instructions for hand washing when water is unavailable, and warnings about flammability and external use only. Directions include pressing the pump twice and rubbing hands together until dry. Additional details cover storage, possible fabric discoloration, and inactive ingredients such as water, cellulosic polymer, and zinc pyrithione.*
FDA Label Image

75209-011-02 2000ml (75209 011 02 2000ml)

75209-011-02 2000ml (75209 011 02 2000ml)
Label of ZaPro Hand Sanitizer showing its professional strength formula with 67.6 fluid ounces (2 liters) net quantity. The label highlights key features such as disinfecting through residual bio-fluid contamination, non-tacky formula, and no sticky residue. It includes a Drug Facts panel listing Ethyl Alcohol 94% as the active ingredient, usage instructions, warnings, inactive ingredients, and contact information. Manufactured by CAO Group Inc.*

* 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.