Triderma Pain Relief Cream
FDA Label NDC 10738-073

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Genuine Virgin Aloe Corporation for the product Triderma Pain Relief (NDC 10738-073). 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 drug facts, active ingredients, purpose, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.