Altachlore Sodium Chloride Hypertonicity

Altachlore Sodium Chloride Hypertonicity is an FDA drug label for the active ingredient SODIUM CHLORIDE manufactured by Altaire Pharmaceuticals Inc. administered by OPHTHALMIC. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231209.

Generic: SODIUM CHLORIDE

Manufacturer: Altaire Pharmaceuticals Inc.

Product Type: HUMAN OTC DRUG

Route: OPHTHALMIC

Dosage Form:

NDC: 59390-183

Application: M018

Effective: 20231209

Active Ingredients: Active ingredient Sodium Chloride 5%

Indications & Usage

Use For the temporary relief of corneal edema.

Dosage & Administration

Directions instill 1 or 2 drops in the affected eye(s) every 3 to 4 hours, or as directed by a doctor.

Contraindications

Not available.

Warnings

Warnings For use in the eyes only Save box for complete information Do not use except under the advice and supervision of a doctor. if solution changes color or becomes cloudy. When using this product keep tightly closed. to avoid contamination, do not touch tip of container to any surface. replace cap immediately after each use. this product may cause temporary burning and irritation on being instilled into the eye. Stop use and ask a doctor if you experience eye pain. changes in your vision occur. continued redness or irritation of the eye persists. condition worsens or persists. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away.

Adverse Reactions

Not available.

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