Dubble Bubble Original Flavor Bubble Gum Hydrating Hand Sanitizer Liquid
Product Images NDC 73928-217

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 Dubble Bubble Original Flavor Bubble Gum Hydrating Hand Sanitizer (NDC 73928-217). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kingkey Mbc Life Technology Group 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

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Front and back views of a yellow pouch containing DUBBLE BUBBLE ORIGINAL FLAVOR BUBBLE GUM Hydrating Hand Sanitizer. The front shows the sanitizer in a clear spray bottle with a red nozzle cap, labeled with the Dubble Bubble logo and product name. The bottle contains 1.2 FL OZ (35 ml) of liquid. The back includes Drug Facts, usage instructions, warnings, and other details in black text on a yellow background. The labeler is Kingkey MBC Life Technology Group Co., Ltd.*
FDA Label Image

Label (Dubble Bubble Original Flavor Bubble Gum Hydrating Hand Sanitizer Compressed)

Label (Dubble Bubble Original Flavor Bubble Gum Hydrating Hand Sanitizer Compressed)
Front and back of DUBBLE BUBBLE ORIGINAL FLAVOR BUBBLE GUM Hydrating Hand Sanitizer in liquid form. The front shows a yellow pouch with a clear bottle and red cap inside, labeled with the brand and flavor. The back has the Drug Facts panel listing active ingredient as 62% alcohol antiseptic, usage instructions, warnings, inactive ingredients, and contact info. The product is labeled as 1.2 FL OZ (35 mL) and is manufactured by Kingkey MBC Life Technology Group 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.