Luzen Whitening Gel
FDA Label NDC 70812-010

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Biostech Co., Ltd. for the product Luzen Whitening Gel (NDC 70812-010). 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 dosage & administration, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Dosage & Administration

for external use only

Warnings

for external use only

keep out of reach children

Package Label.Principal Display Panel

Label (Label)

Label (Label)

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