Sodium Chloride
- Dosage form
- SOLUTION/ DROPS
- Labeler
- Akorn
- Label updated
- 2022-07-01
- Retrieved
- 2026-09-07
- Active ingredients
- Sodium Chloride
Label information
Drug Facts
Active ingredient
Sodium Chloride 5%
Purpose
Hypertonicity Agent
Use
- for temporary relief of corneal edema.
Warnings
Label information
Do not use
- this product except under the advice and supervision of a doctor.
- if imprinted seal is broken or missing.
- if solution changes color or becomes cloudy.
Label information
When using this product
- temporary burning and irritation upon being instilled into eye may occur.
- to avoid contamination, do not touch tip of container to any surface
- replace cap after each use
Label information
Stop use and ask a doctor if
- you experience eye pain.
- you experience changes in vision.
- redness or irritation of the eye continues
- condition worsens or persists.
Label information
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Instill 1 or 2 drops in the affected eye(s) as needed.
Other information
- Store at 20° to 25°C (68° to77°F) [see USP Controlled Room Temperature].
- Keep tightly closed.
Inactive ingredients
Boric Acid, Hypromellose 2906, Methylparaben 0.23 mg (0.023%), Propylparaben 0.1 mg (0.01%), Propylene Glycol, Sodium Borate, Sodium Hydroxide and/or Hydrochloric Acid to adjust pH (6.0 to 8.0), and Water for Injection.
포장 표시
Principal Display Panel Text for Container Label:
NDC 17478-623-12
5%
SODIUM
CHLORIDE
Ophthalmic
Solution, USP
Hypertonicity
Eye Drops
15 mL (0.5 fl. oz.) Sterile
[Image in the official label — see DailyMed source]
포장 표시
Principal Display Panel Text for Carton Label:
NDC 17478-623-12
5%
SODIUM
CHLORIDE
Ophthalmic
Solution, USP
Hypertonicity Eye Drops
Comparable to Muro-128®*
15 mL (0.5 fl. oz.) Sterile
Akorn Logo
[Image in the official label — see DailyMed source]
DailyMed Set ID: ab12c419-4b1a-4119-9e23-76ce7a89d1a7 · Version 8
NDC: 17478-623