Carboxymethylcellulose Sodium Eye Drops 0.5% For Solution
FDA Label NDC 16030-501

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Aurolab for the product Carboxymethylcellulose Sodium Eye Drops 0.5% (NDC 16030-501). 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, directions for use, inactive ingredient, tamper protection, use, questions, keep out of reach of children, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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