FDA Label for Sodium Chloride
View Indications, Usage & Precautions
Sodium Chloride Product Label
The following document was submitted to the FDA by the labeler of this product Walgreen Company. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Sodium Chloride 5%
Purpose
Hypertonicity Agent
Use
• For the temporary relief of corneal edema.
Warnings
For use in the eyes only
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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.
Directions
• instill 1 or 2 drops in the affected eye(s) every 3 to 4 hours, or as directed by a doctor.
Other Information
• replace cap after using and keep tightly closed.
• store at 15° to 30°C (59° to 86°F).
• remove contact lenses before using.
Inactive Ingredients
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.
Questions?
• 1-800-925-4733 • 9am – 5pm EST Monday - Friday
Principal Display Panel
Walgreens
NDC 0363-0193-13
Sodium Chloride
Ophthalmic
Solution, 5%
Hypertonicity
Eye Drops
0.5 FL OZ (15 mL)
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