Alcohol Hand Sanitizer
Product Images NDC 78792-012

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Alcohol Hand Sanitizer (NDC 78792-012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guangdong Theaoson Technology 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

78792-012-01 50ml (78792 012 01 50ml)

Label for ALCOHOL HAND SANITIZER with 75% alcohol content, 1.79 fl. oz (50 ml) bottle, manufactured by GUANGDONG THEAOSON TECHNOLOGY CO., LTD. The label highlights antiseptic use, flammability warning, directions, and storage instructions. It includes contact information and safety certifications and indicates the product is made in China.*

FDA Label Image

78792-012-02 100ml (78792 012 02 100ml)

ALCOHOL HAND SANITIZER 75% alcohol 3.4 FL.oz / 100mL by GUANGDONG THEAOSON TECHNOLOGY CO.,LTD features a green label with a droplet indicating 75% alcohol content. The label includes warnings about flammability, usage instructions, active and inactive ingredients, and storage information. The product is made in China and displays various certification marks and a barcode.*

FDA Label Image

78792-012-03 182ml (78792 012 03 182ml)

Label for ALCOHOL HAND SANITIZER by GUANGDONG THEAOSON TECHNOLOGY CO., LTD, showing 75% alcohol content. The label includes product name, volume of 6.16 FL.oz / 182 ML, flammable warning, usage directions, active ingredient alcohol 75%, safety instructions, and manufacturing details. The label is predominantly green and white with a red THEAOSON logo.*

FDA Label Image

78792-012-04 478ml (78792 012 04 478ml)

Label for THEAOSON Alcohol Hand Sanitizer gel with 75% alcohol content, containing 16.15 FL.oz (478 mL). The label highlights antiseptic use, cautions against use on young children and damaged skin, and warns it is flammable. It includes manufacturer Guangdong THEAOSON Technology Co., Ltd information and safety symbols, with storage and use directions, and a barcode. The product is made in China.*

FDA Label Image

78792-012-05 494ml (78792 012 05 494ml)

ALCOHOL HAND SANITIZER 16.72 FL. OZ. (494 mL) by GUANGDONG THEAOSON TECHNOLOGY CO.,LTD. The green front label features a cartoon yellow character washing hands with soap bubbles and an Aloe graphic, highlighting moisturizing antibacterial properties. The back label lists active ingredient Alcohol 75% (v/v) as an antiseptic, warnings, directions, inactive ingredients, and company contact details, along with safety and quality certification logos and a barcode.*

FDA Label Image

78792-012-06 1000ml (78792 012 06 1000ml)

Packaging label for THEAOSON Alcohol Hand Sanitizer Gel containing 75% alcohol, with a volume of 35.72 FL. oz / 1 L. The front label highlights its germ-killing effectiveness and features icons for antibacterial, moisturizing, sterilization, and rinse-free attributes. The back label includes active ingredient details, warnings, directions, storage information, manufacturer contact, and certification logos. The product is manufactured by GUANGDONG THEAOSON TECHNOLOGY CO., LTD and made in China.*

FDA Label Image

78792-012-07 5000ml (78792 012 07 5000ml)

ALCOHOL HAND SANITIZER gel with 75% alcohol by GUANGDONG THEAOSON TECHNOLOGY CO., LTD, presented in a 171 FL.oz / 5L container. The front label highlights its ability to kill 99.99% of germs and features icons indicating cleanliness, antibacterial effect, gentle moisturizing, sterilization, and being rinse-free. The back label includes active ingredients, usage instructions, warnings, manufacturer details, and certification marks, with a barcode and country of origin marked as Made in China.*

* 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.