Disney Pixar Lightyear Hand Sanitizer
Product Images NDC 74530-061

2 FDA label images from Best Brand Consumers Products, Inc. · 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 Disney Pixar Lightyear Hand Sanitizer (NDC 74530-061). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Best Brand Consumers Products, Inc., 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 Description (Image 20220111115137)

Image Description (Image 20220111115137)
Drug Facts panels for Disney PIXAR LIGHTYEAR HAND SANITIZER distributed by Best Brand Consumers Products, Inc. The active ingredient is Ethyl Alcohol 68% as an antiseptic. Uses include decreasing bacteria on skin to prevent disease, recommended for repeated use. Warnings address external use, flammability, eye contact, inhalation, ingestion, and keeping out of children's reach. Directions include applying to wet hands and supervision for children under 6. Other information advises against storage above 105°F. Inactive ingredients listed are water, glycerin, propylene glycol, carbomer, and sodium hydroxide, with a contact number for questions.*
FDA Label Image

Image Description (Image 20220111115200)

Image Description (Image 20220111115200)
Front label of Disney PIXAR LIGHTYEAR HAND SANITIZER showing a close-up image of the Lightyear character in space-themed armor. The label includes the text 'HAND SANITIZER' and the volume '2 fl. oz/60 mL'. The bottle is clear with a transparent flip-top cap. Labeled by Best Brand Consumers Products, Inc.*

* 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.