Touchland X Hello Kitty Power Mist Hand Sanitizer Berry Bliss Mist Case Spray
Product Images NDC 72033-144

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Touchland X Hello Kitty Power Mist Hand Sanitizer Berry Bliss Mist Case (NDC 72033-144). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Touchland 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

Inner Package2 (Inner Package2)

Inner Package2 (Inner Package2)
This image shows the warnings, active and inactive ingredients, and directions for Touchland x Hello Kitty Power Mist Hand Sanitizer Berry Bliss Mist Case. It lists Alcohol 70% v/v as the active ingredient, includes detailed warnings about flammability and contact precautions, and instructs to spray onto hands and rub until dry. The product is berry bliss scented and distributed by Touchland LLC.*
FDA Label Image

Outer Package2 (Outer Package2)

Outer Package2 (Outer Package2)
Touchland x Hello Kitty Power Mist Hand Sanitizer Berry Bliss Mist Case packaging label. The label features a red background with repeated Hello Kitty head illustrations wearing red bows. It displays the product name, Berry Bliss Power Mist + Mist Case, and identifies the product as a hydrating hand sanitizer spray with 1 fl oz (30 mL) providing 500 sprays. The back panel includes drug facts listing Alcohol 70% v/v as the active ingredient, usage warnings, directions, inactive ingredients, and branding elements by Touchland LLC and Sanrio. The label also highlights features such as fast absorbing, cruelty-free, and net zero plastic waste brand.*

* 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.