Hand Sanitizer Gel
Product Images NDC 41366-017

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 41366-017). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zhejiang Meimi 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

89ml Label_1 (89ml 1)

Label artwork for Hand Sanitizer gel, cucumber and melon scented, in a 3 fl oz (89 mL) size. The front shows the product name with an image of watermelon and cucumber slices. The back displays a detailed Drug Facts panel with active ingredient Ethyl Alcohol 70% v/v, usage instructions, warnings, inactive ingredients, and distributor information (Fourstar Group USA, Inc.). Dimensions are 72 mm by 37 mm.*

FDA Label Image

89ml Label_2 (89ml 2)

Label design for Hand Sanitizer gel by Zhejiang Meimi Technology Co., Ltd. Front label shows "Hand Sanitizer" 3 FL. OZ (89 mL) with coconut and lime scent and image of a coconut half and lime slice. Back label contains Drug Facts including active ingredient ethyl alcohol 70% v/v and warnings. Distributed by Fourstar Group USA, Inc., made in China.*

FDA Label Image

89ml Label_3 (89ml 3)

Hand Sanitizer anti-bacterial hand gel in a 89 mL (3 fl oz) pouch with pomegranate and vanilla scent. The front features the product name and scent description over an image of pomegranate and vanilla flowers. The back displays a Drug Facts panel listing ethyl alcohol 70% v/v as the active ingredient and includes warnings, directions, and inactive ingredients. The labeler is Zhejiang Meimi Technology Co., Ltd.*

* 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.