Steady Freddy Spray
Product Images NDC 82191-001

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 Steady Freddy (NDC 82191-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Symbiosis Pty Ltd, 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

Inactive Ingredients (Steady Freddy Inactives)

Inactive Ingredients (Steady Freddy Inactives)
Drug Facts panel listing active ingredients including Alcohol, Caprylic/Capric Triglycerides, Isopropyl Myristate, PEG-40 Stearate, Sodium Saccharin, and Water/Aqua for Steady Freddy topical spray.*
FDA Label Image

Steady Freddy (Steady Freddy Label Final Jpg)

Steady Freddy (Steady Freddy Label   Final Jpg)
Steady Freddy 96 mg/mL Lidocaine Spray Solution label for male genital desensitizer. The label states it contains 80 sprays in a 0.35 fl oz (10 mL) container, distributed by Medical Symbiosis Pty Ltd, Bondi Beach NSW, Australia. It includes warnings, directions, ingredients such as Lidocaine 9.6% w/v, inactive ingredients, and storage instructions. Made in Australia.*
FDA Label Image

Warnings (Steady Freddy Warnings (2))

Warnings (Steady Freddy Warnings (2))
Drug facts and warning label panel for Steady Freddy Lidocaine 96 mg/mL topical spray by Medical Symbiosis Pty Ltd. It includes safety warnings such as potential flammability and advice to avoid use on broken or irritated skin, not to spray in eyes or nostrils, and to keep out of reach of children. Use under medical supervision is recommended if symptoms persist beyond three months.*

* 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.