Baja Blast Hand Sanitizing Wipes Cloth
Product Images NDC 85844-503

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 Baja Blast Hand Sanitizing Wipes (NDC 85844-503). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zhejiang Bright Care 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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The packaging label for BAJA BLAST HAND SANITIZING WIPES features the Mountain Dew Baja Blast logo prominently on a teal background with the text 'Hand Sanitizing Wipes 20CT' below. The label includes a Drug Facts panel detailing active ingredient benzalkonium chloride 0.13%, uses, warnings, directions, inactive ingredients, and a contact number for questions. A barcode and manufacturer details (Zhejiang Bright Care Co., Ltd) are also visible. The label design dimensions and color codes are shown, with a final appearance image depicting the wipes container shaped like a Mountain Dew can.*
FDA Label Image

Label (Baja Blast Hand Sani Wipes Compressed)

Label (Baja Blast Hand Sani Wipes Compressed)
Packaging label for BAJA BLAST HAND SANITIZING WIPES by Zhejiang Bright Care Co., Ltd. The label features a teal background with the Mountain Dew Baja Blast logo prominently displayed. It specifies the product as hand sanitizing wipes, 20 count. The label includes a Drug Facts section detailing active ingredients, uses, warnings, directions, inactive ingredients, and a contact phone number. Color codes and dimensions are also visible in the design layout.*

* 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.