Uauko Fungal Nail Treatment Liquid
FDA Label NDC 87408-018

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Jingliang Cosmetics Co., Ltd. for the product Uauko Fungal Nail Treatment (NDC 87408-018). 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, purpose, uses, ask doctor, warnings, do not use, keep oot of reach of children, stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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