Instant Hand Antiseptic Gel
Product Images NDC 59448-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Instant Hand Antiseptic (NDC 59448-001). 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 (53 mL Bottle Label)

Northside Hospital Instant Hand Antiseptic 62% w/w Ethyl Alcohol 53 mL bottle label distributed by ASP Global, LLC. The label features product name, active ingredient concentration, volume, and company address. The label includes usage instructions and formulation details, indicating it is used as a hand antiseptic.*

FDA Label Image

Principal Display Panel (10 g Tube Label)

Drug Facts panel for Colgate Cavity Protection toothpaste, active ingredient sodium monofluorophosphate 0.76% (0.15% w/v fluoride ion) as anticavity agent. Includes usage instructions, warnings for children under 6, directions for brushing by age groups, and inactive ingredients list. Contact information for questions is also provided.*

FDA Label Image

Principal Display Panel (Kit Label)

Northside Hospital Mothers Vaginal Kit, containing ALCOHOL and SODIUM MONOFLUOROPHOSPHATE in a 62 mL/100 mL kit form by ASP Global, LLC. The image shows a blue insulated bag with the Northside Hospital logo, four small bottles inside (including alcohol-free mouthwash and body lotion), and a larger dark-colored mother’s bag with the same branding. The accompanying labels detail kit contents, including toiletries, sanitary pads, a cleansing bottle, a cup, and perineal instant cold packs.*

* 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.