Hand Sanitizer
Product Images NDC 75647-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75647-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Verico Technology, 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

236 mL Label (236 mL Label)

Label for Hand Sanitizer by Verico Technology, for an 8 oz (236 mL) bottle. The label features a blue medical cross symbol, with "HAND SANITIZER" prominently displayed and the description "Color Free, Scent Free." It lists the active ingredient as Isopropyl Alcohol Antiseptic 75%, topical and non-sterile solution. The label includes a Drug Facts panel with detailed usage, warnings, directions, and inactive ingredients information.*

FDA Label Image

354 mL Label (354 mL Label)

Label for Verico Technology Hand Sanitizer, 12 oz (354 mL) bottle. The label indicates it is color free, scent free, and contains isopropyl alcohol antiseptic 75%, a topical, non-sterile solution. The label includes a Drug Facts panel with active ingredient, uses, warnings, directions, and other information.*

FDA Label Image

A58980f4 B187 6d6d E053 2a95a90a85db

Label design for Hand Sanitizer by Verico Technology, sized for a 32 oz (946 mL) bottle. The label highlights that the product is color and scent free, an alcohol antiseptic 80% topical non-sterile solution. It includes a Drug Facts box with active ingredient Alcohol 80% v/v, usage instructions, warnings, directions, and inactive ingredients. The label also includes contact information for Verico Technology and color specifications for printing.*

* 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.