Relieved Pro Wrap Patch
FDA Label NDC 71662-004

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Transfer Technology for the product Relieved Pro Wrap (NDC 71662-004). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, use, indications and usage, warnings, do not use, ask your doctor, when using this product, stop use if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

* Please review the disclaimer below.