Preboost
Product Images NDC 62192-8500

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Preboost (NDC 62192-8500). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by 944 Corp, 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 – Pouch Label (Pre0d 0000 01)

Preboost male desensitizing wipes, single-use premoistened towelette. Contains Benzocaine USP 4% as the active ingredient. The label highlights its purpose in temporarily prolonging time until ejaculation. Developed by Dr. Harry Fisch and manufactured for 944 Corp, located in New York, NY. The label includes directions for use, warnings, active and inactive ingredients, and a website link www.preboost.com.*

FDA Label Image

Principal Display Panel – Box Label (Pre0d 0000 02)

Preboost Male Desensitizing Wipes package label featuring 10 single-use premoistened towelettes for male desensitization. The active ingredient is Benzocaine USP 4%. Manufactured for 944 Corp, the label includes branding, usage directions, warnings, and contact information.*

* 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.