Active Ingredient
Sodium Chloride 5%
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Company for the product Sodium Chloride (NDC 0363-0193). 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, purpose, use, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Sodium Chloride 5%
Hypertonicity Agent
• For the temporary relief of corneal edema.
For use in the eyes only
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• except under the advice and supervision of a doctor.
• if solution changes color or becomes cloudy.
• 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.
• you experience eye pain. • changes in your vision occur.
• continued redness or irritation of the eye persists.
• condition worsens or persists.
If swallowed, get medical help or contact a Poison Control Center right away.
• instill 1 or 2 drops in the affected eye(s) every 3 to 4 hours, or as directed by a doctor.
• replace cap after using and keep tightly closed.
• store at 15° to 30°C (59° to 86°F).
• remove contact lenses before using.
Boric Acid, Hypromellose, Methylparaben, Propylene Glycol, Propylparaben, Sodium Borate, and Water for injection. Sodium Hydroxide and/or Hydrochloric Acid may be added to adjust pH.
• 1-800-925-4733 • 9am – 5pm EST Monday - Friday
Walgreens
NDC 0363-0193-13
Sodium Chloride
Ophthalmic
Solution, 5%
Hypertonicity
Eye Drops
0.5 FL OZ (15 mL)
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