Painbloc24 Flexi-stretch Pain Tape
Product Images NDC 71226-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Painbloc24 Flexi-stretch Pain Tape (NDC 71226-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vizuri Health Sciences Llc, 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

Image 1

This appears to be a product label for a foot pain relief patch. It contains instructions for use ("Note: Will use gloss finish on complete outside of carton"), a product name ("FLEXI-STRETCH TS FOOT PAIN PATCH"), a tagline ("Relief that Sticks!"), a product description ("MAX STRENGTH FORMULA"), and a percentage of active ingredient ("LIDOCAINE 4%"). There is also a warning regarding packaging not being child-resistant.*

FDA Label Image

New Label 3

The provided text seems to include a mix of random characters along with some sections discussing a pain relief patch called "PainBloc24" that has technology designed to adhere to moving joints and provide relief for up to 12 hours. The patch is formulated with natural ingredients and can be used on various areas such as knees, back, shoulders, and elbows.*

FDA Label Image

New Label 2

MAX STRENGTH FORMULA HA is a back pain tape that contains Lidocaine 4% for numbing pain relief for up to 2 hours. It is a flexible tape designed to move with your body and stay in place. This tape is intended for use on large pain areas on the back. The revolutionary fabric used in the tape is created to ensure the tape stays in place during activities. The formula is created for maximum strength and is designed to care for safety. Drug facts are also present on the packaging.*

* 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.