Tattoogirl Numbing Cream
Product Images NDC 70171-0021

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Tattoogirl Numbing (NDC 70171-0021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Prodigy Media 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

Tattoo_girl_1oz Box.jpg (Tattoo Girl 1oz Box)

This product is an external pain relief cream containing ingredients like Arnica Montana Flower Extract, Chondroitin Sulfate, Emu Oil, and Tea Tree Oil. It is intended for adults and children over 2 years old to apply to affected areas up to 3 to 4 times daily. Warnings include avoiding contact with eyes, not using on wounds or damaged skin, and seeking medical advice if symptoms persist. Additionally, the product is not tested on animals and advises contacting a Poison Control Center if swallowed. For product-related inquiries, contact 866-750-4669.*

FDA Label Image

Tattoo_girl_1oz Label.jpg (Tattoo Girl 1oz Label)

This product is an external analgesic containing Lidocaine HCL 4.0% w/w as the active ingredient. It also includes various inactive ingredients such as Arnica Montana Flower Extract, Chondroitin Sulfate, and Emu Oil. It is recommended for adults and children over 2 years old to apply to the affected area no more than 3 to 4 times daily. The warning includes avoiding contact with eyes and seeking medical attention if the condition worsens. The product should not be used on wounds or damaged skin. If swallowed, medical assistance should be sought immediately. The product should not be used if the seal is broken.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.