Drug Facts Fusoni Hand Sanitizer Plus Blue (Drug Facts Fusoni Hand Sanitizer Plus Blue)
Fusoni Hand Sanitizer With Moisturizer Plus
Product Images NDC 79380-011
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Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fusoni Hand Sanitizer With Moisturizer Plus (NDC 79380-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Fusoni S.a. De C.v., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Drug Facts Fusoni Hand Sanitizer Plus (Drug Facts Fusoni Hand Sanitizer Plus)
This is a drug facts label for a hand sanitizer that contains 70% ethyl alcohol as an antimicrobial agent. It is recommended for repeated use to decrease bacteria on the skin that could cause disease. The label warns that the product is flammable and should be kept away from a heat source or fire. It is for external use only and should not be inhaled or ingested. The hand sanitizer should not be used near the eyes or on broken skin. If contact with the eyes occurs, rinse thoroughly with water. Children under six should be supervised while using this product. The inactive ingredients include water, hydroxyethylcellulose, PPG-3 benzyl ether myristate, citric acid, phenoxyethandl, glycerin, and ammonium hydroxide. The product should not be stored above 109°F (43°C) and may discolor certain fabrics or surfaces.*
Front Label Fusoni Hand Sanitizer Plus (Front Label Plus 1gal)
The text appears to be a location description that says "Tutlitlén, Edo. de Mex" which refers to an area in the State of Mexico, Mexico.*
Front Label Fusoni Hand Sanitizer Plus Blue (Front Label Plus Blue 1 Gal)
* 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.
