Dream Eye
FDA Label NDC 52345-7001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by K&j.c Co., Ltd for the product Dream Eye (NDC 52345-7001). 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 description, dosage & administration, otc - keep out of reach of children, otc - purpose, warnings, inactive ingredient, otc - active ingredient, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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