Sodium Chloride Ophthalmic 5 Percent Hypertonicity Eye Ointment
FDA Label NDC 11716-0750

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hanlim for the product Sodium Chloride Ophthalmic 5 Percent Hypertonicity Eye (NDC 11716-0750). 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 other, active ingredient, purpose, use, warnings, do not use, when using this product, stop use and ask a doctorif, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Do Not Use

this product except under the advice and supervision of a doctor.

When Using This Product

• avoid contamination, do not touch tip of container to any surface.

• replace cap after use.

• this product may cause temporary burning and irritation on being instilled into the eye.

Stop Use And Ask A Doctorif

• you experience eye pain, changes in vision, continued redness or irritation of the eye.

• condition worsens or persists for more than 72 hours.

Keep This And All Drugs Out Of The Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

* Please review the disclaimer below.