Foasu Daily Hand Sanitizer Gel
Product Images NDC 77964-001

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Foasu Daily Hand Sanitizer Gel (NDC 77964-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hanscos 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.

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FDA Label Image

Product Label (Hand Sannitizer)

Product Label (Hand Sannitizer)
This product is a hand sanitizer manufactured by Hanscos Co., Ltd. The bottle contains 16.9 fluid ounces or 500 ml of the solution. It contains 70% ethyl alcohol and is intended to reduce bacteria on the skin. The product is flammable and should be kept away from fire or flames. It should only be used externally and should not be used near the eyes. Individuals under the age of 5 should be supervised when using the product. If irritation or rash appears and lasts, individuals should stop using the product and consult a doctor. If swallowed, medical help should be sought, or the Poison Control Center should be contacted immediately. The product should be stored below 110°F (63°C) and may discolor certain fabrics or surfaces. The inactive ingredients include water, glycerin, PEG-60 hydrogenated castor oil, carbomer, tromethamine, camellia sinensis leaf extract, aloe barbadensis leaf extract, mentha piperita (peppermint) oil, and limonene.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.