Tattoo Goo
Product Images NDC 43689-0056

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Tattoo Goo (NDC 43689-0056). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Magni Group 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 Goo Dfp 59.15 mL (Tattoo Goo Dfp Final 59.15ml)

Drug Facts label for Tattoo Goo by The Magni Group, Inc. Active ingredient is Chloroxylenol 0.5% as an antibacterial. The label includes use instructions, warnings, directions for application, and a list of inactive ingredients such as water, sodium PEG-7 olive oil carboxylate, propanediol, olive oil PEG-7 esters, and others. Also displayed are manufacturer addresses in the USA and the UK, a barcode, a 24-month shelf life symbol, and the product volume of 59.15 ml.*

FDA Label Image

Tattoo Goo Pdp 59.15ml (Tattoo Goo Pdp Final 59.15ml)

Tattoo Goo Deep Cleansing Soap for Tattoos & Piercings label displaying antibacterial, antimicrobial, and pH balanced properties. The packaging highlights the Advanced PCMX-L Micro Molecular Formula. The product volume is 2 oz (59.15 ml), and it is made in the USA by The Magni Group Inc.*

* 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.