Instant Erection Cream
Product Images NDC 83608-104

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Instant Erection (NDC 83608-104). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novelties By Nasswalk, Inc., 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

Tube (Instant Erection Tube 0.5 Oz)

Label for Instant Erection Cream, a topical cream containing 5 g/100 mL of Ultimate Erection Enhancer. The label features a black background with a yellow oval containing the product name. It lists the active ingredient Benzocaine 5%, states the purpose as a desensitizer, and includes directions, warnings, and inactive ingredients. Distributed by Novelties by Nasswalk, Inc.*

FDA Label Image

Unit Carton-1 (Instant Erection Uc 0.5 Oz)

Label for Instant Erection Cream, a topical OTC drug by Novelties by Nasswalk, Inc. The label highlights the active ingredient Benzocaine 5% as a desensitizer, with the generic name Ultimate Erection Enhancer. The label includes drug facts, directions for use, and a barcode, with a red and yellow flame-themed design.*

FDA Label Image

Unit Carton-2 (Instant Erection Uc 2 0.5 Oz)

Instant Erection Cream topical cream, 5 g/100mL strength, labeled as Ultimate Erection Enhancer. Packaging displays product name prominently in bold, red and white text on black background. Manufacturer is Novelties by Nasswalk, Inc. The label includes drug facts noting Benzocaine 5% as the active ingredient, with uses, warnings, and directions. Barcode and product NDC visible. The design also features a graphic image and company logo.*

* 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.