Instant Hand Antiseptic Gel
Product Images NDC 59448-003

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Instant Hand Antiseptic (NDC 59448-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asp Global, 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

Principal Display Panel (10 g Tube Label)

Drug Facts panel for toothpaste, showing active ingredient Sodium monofluorophosphate 0.76% (0.15% w/v fluoride ion) as anticavity. Includes usage instructions, warnings for children under 6, directions by age group, and a list of inactive ingredients. Also provides a contact number for questions or comments.*

FDA Label Image

Principal Display Panel (53 mL Bottle Label)

Label for Univ of Vermont Medical Center Amenity Instant Hand Antiseptic kit by ASP Global, LLC. The front shows the product name ‘‘Instant Hand Antiseptic’’ noting it is alcohol and fragrance free, with a volume of 1.9 FL OZ (53 mL). The back includes a Drug Facts panel listing Benzalkonium Chloride 0.095% as the active ingredient, its antiseptic use, warnings, directions for use, and inactive ingredients. The product is made in China.*

FDA Label Image

Principal Display Panel (Kit Label)

The Univ of Vermont Medical Center Amenity Kit is a green, zippered pouch measuring approximately 13.8 cm wide, distributed by ASP Global, LLC. The kit includes a 1.9 fl. oz. alcohol and fragrance-free hand sanitizer, 0.15 oz. lip balm, toothbrush, sleep mask, ear plugs, notebook, pen, and a kit case. Components are made in China, with toothpaste manufactured in Thailand. The label displays lot number and expiration date placeholders and indicates assembly in China.*

* 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.