Mugwort Patch
FDA Label NDC 85136-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Henan Toudaorong Biotechnology Co., Ltd. for the product Mugwort (NDC 85136-001). 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 (strength), inactive ingredients, purpose, otc - keep out of reach of children section, indications & usage section, warnings section, dosage & administration section, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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