Sodium Chloride description, usages, side effects, indications, overdosage, supplying and lots more!

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Sodium Chloride

CVS Pharmacy
Akorn, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredient

Sodium Chloride 5%

Purpose

Hypertonicity Agent

Use

  • For the temporary relief of corneal edema

Warnings

Do not use

  • this product except under the advice and supervision of a doctor
  • if solution changes color or becomes cloudy

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

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

Keep out of reach of children.

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

Questions or comments?

1-800-932-5676

Directions

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

Other information

  • store at 20° to 25°C (68° to 77°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 Purified Water USP.

Principal Display Panel Text for Container Label:

CVS

pharmacy™

NDC 59779-382-01

Ophthalmic Solution

SODIUM

CHLORIDE

USP, 5%

HYPERTONICITY

EYE DROPS

15 mL (0.5 FL OZ)

STERILE

Principal Display Panel Text for Carton Label:

CVS

pharmacy™

NDC 59779-382-01

Compare to the active

ingredient in Muro® 128*

NEW!

Ophthalmic Solution

SODIUM

CHLORIDE

USP, 5%

HYPERTONICITY

EYE DROPS

● Temporary relief of

corneal edema

● Doctor recommended

15 mL (0.5 FL OZ) STERILE

Sodium Chloride

Sodium Chloride SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59779-382
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM CHLORIDE 50 mg

Inactive Ingredients

Ingredient Name Strength
BORIC ACID
Hypromellose 2906 (4 mpa.s)
propylene glycol
SODIUM BORATE
SODIUM HYDROXIDE
HYDROCHLORIC ACID
water
METHYLPARABEN
PROPYLPARABEN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, DROPPER
2 NDC:59779-382-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-06-14


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Be sure to consult your doctor before taking any medication!
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