Mentol Ice Gel
FDA Label NDC 78192-500

11 label sections · Submitted to the FDA by Boe Dominicana Srl · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Boe Dominicana Srl for the product Mentol Ice Gel (NDC 78192-500). 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 ingredients / ingredientes activos, purpose / propósito, uses / usos, warnings / advertencias, when using this product / al usar este producto, stop using and consult a doctor if: / suspender su uso y consultar a un médico si:, keep out of reach of children / mantener fuera del alcance de los niños, directions / modo de uso, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

* Please review the disclaimer below.