Wellnicity Hand Sanitizer
Product Images NDC 62400-0017

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Wellnicity Hand Sanitizer (NDC 62400-0017). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by United Laboratories Manufacturing, 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.

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FDA Label Image

Image Description (Box2)

Image Description (Box2)
This is a description of a hand sanitizer product by Wellnicity. It contains 70.0% Ethyl Alcohol as the active ingredient with a purpose of being an antimicrobial agent. The product is for external use only and should not be applied to open wounds or damaged skin. It is advised to keep it away from excessive heat or open flames. In case of eye contact, the user should flush with water. The directions suggest applying the entire packet to the palm of the hand and rubbing until hands are completely covered. The hand sanitizer helps reduce bacteria on the skin that could cause disease. The product is sourced, formulated, quality tested, and distributed by Wellnicity in Austin, TX. Additionally, the ingredient list includes Distilled Water, Biopol Plus / Carbomer 940, Aloe Vera Aqueous Extract, Aminomethyl Propane, and Rapidgel.*

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