Mdp Peptide 9 Bio Sun Pro Stick
FDA Label NDC 72220-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Skinidea Co., Ltd for the product Mdp Peptide 9 Bio Sun Pro (NDC 72220-002). 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 otc - active ingredient, inactive ingredient, otc - purpose, warnings, indications & usage, dosage & administration, description, 72220-002-02: mdp peptide 9 bio sun stick pro (version 1), and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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