Wave Hand Sanitizer
Product Images NDC 77566-831

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Wave Hand Sanitizer (NDC 77566-831). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Earthlite, Llc, 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

Wave 8 (Wave Hand Sanitizer 8oz Label)

This is a liquid spray antiseptic with 80% alcohol content as the active ingredient to reduce bacteria that may cause disease. It is a CDC recommended formula that is FDA registered. It is suitable for external use and should be kept away from children below 2 months. It should not be used on open skin wounds or ingested. The product should be rubbed on all surfaces of the hand until it is dry. The inactive ingredients include Blood Orange Pecl Oil, Bourbon Vanilla Bean Oil, Cardamom Seed Extact, Cedarwood, and other extracts. It is manufactured and distributed in the USA by Tara Spa Therapy.*

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