Hand Sanitizer
Product Images NDC 78837-202

3 FDA label images from Phoenix Wipes Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 78837-202). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Phoenix Wipes 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

Active Ingredient (Label)

Active Ingredient (Label)
Drug Facts panel for Hand Sanitizer by Phoenix Wipes Inc, listing ethanol 70% as the active antiseptic ingredient. The label includes uses, warnings, directions for application, and safety instructions, such as keeping out of reach of children and avoiding eye contact. Contact information for questions is also provided.*
FDA Label Image

Package Picture (Princiable Display Panel)

Package Picture (Princiable Display Panel)
Packaging label for Phoenix Wipes Hand Sanitizer. The label highlights Instant Hand Sanitizer in antibacterial pocket size packaging, containing 0.067 fluid ounces (2 milliliters) per wipe. The label also states it kills 99% of germs and features the Phoenix Wipes logo with a stylized orange phoenix.*
FDA Label Image

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A7a013f1 D5e3 5cf5 E053 2995a90ad9b7
Packaging label for Phoenix Wipes Instant Hand Sanitizer single wipe. The label highlights 1 antibacterial pocket-size wipe containing 0.067 fluid ounces (2 mL) of sanitizer and claims to kill 99% of germs. The design features the Phoenix Wipes logo with orange and red curved accents on a white textured background.*

* 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.