Men Delay Wipe
Product Images NDC 82659-1000

View Photos of 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 Men Delay Wipe (NDC 82659-1000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Limitless Male Medical Clinic, 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

Label (Kronos)

Label (Kronos)
Packaging label for Men Delay Wipe, a single-use product by Limitless Male Medical Clinic. The front features the brand name KRONOS with the phrase LONG-LASTING SUPPORT and states it contains 1 wipe. The back provides drug facts, active ingredient Benzocaine 3.5%, usage instructions, warnings, and directions for application.*
FDA Label Image

Label (Kronos Box)

Label (Kronos Box)
Packaging label for Kronos Long-Lasting Support male genital desensitizer wipes. The product contains 8 wipes with 3.5% benzocaine and is marketed for fast acting, quick absorbing, and clinically proven effects. The label includes drug facts, usage, warnings, directions, inactive ingredients, a QR code, and a barcode. Manufacturer and address details are present.*
FDA Label Image

Dc640c5e E875 2a74 E053 2995a90a4279

Dc640c5e E875 2a74 E053 2995a90a4279
Packaging label for KRONOS Male Genital Desensitizer wipes. The label highlights the active ingredient as Benzocaine 3.5% and indicates the package contains 8 wipes. The product is described as long-lasting support, fast acting, quick absorbing, clinically proven, and extends climax. The label includes drug facts, warnings, directions, inactive ingredients, and manufacturer information from Limitless Male Medical Clinic.*

* 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.