Terrapure Hand Sanitizer
Product Images NDC 75010-150

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Terrapure Hand Sanitizer (NDC 75010-150). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mirfeel Korea 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

Image Of Bottle (100ml Bottle)

TerraPure HAND SANITIZER gel, 100 ml (3.38 fl. oz.), labeled with 70% Ethyl Alcohol as the active ingredient. The package highlights a White Jasmine Flower scent and uses blue text on a white background. The label includes bilingual (English/French) drug facts, usage instructions, warnings, and inactive ingredients. Distributed by TerraPure Sanitizer Inc., made in Korea, with NPN 80103052.*

FDA Label Image

Image Of Bottle (1litter Bottle)

TerraPure HAND SANITIZER gel with 70% ethyl alcohol, fragrance-free, in a 1-liter (33.81 fl. oz) clear pump bottle. The label includes bilingual text in English and French, highlighting its antiseptic purpose, usage directions, warnings, and inactive ingredients. It is distributed by TerraPure Sanitizer Inc. and made in Korea.*

FDA Label Image

Image Of Bottle (3780ml Bottle)

Label images of TerraPure HAND SANITIZER gel by Mirfeel Korea Co., Ltd display front and back panels in blue and white, along with a white container with a handle and screw cap. The front states the fragrance-free gel contains 70% ethyl alcohol and leaves hands feeling soft, with volume marked 3.78L (127.82 FL. OZ). The back panel includes bilingual Drug Facts, ingredients, safety warnings, usage directions, distributor info, and a QR code.*

* 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.