Elta Md Uv Aox Eye Cream
FDA Label NDC 72043-4342

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cp Skin Health Group, Inc. for the product Elta Md Uv Aox Eye (NDC 72043-4342). 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 directions, warning, inactive ingredient, indications & usage, keep out of reach of children, purpose, elta md uv aox eye, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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