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

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Sodium Chloride

Walgreens
Akorn, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Sodium Chloride 5%

Purpose

Hypertonicity Agent

Use

  • for temporary relief of corneal edema.

Warnings

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.

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.

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 Purified Water USP.

Principal Display Panel Text for Container Label:

Well at

Walgreens NDC 0363-9040-00

STERILE

Sodium Chloride

Ophthalmic

Solution USP, 5%

Hypertonicity Eye Drops

0.5 FL OZ (15 mL)

Principal Display Panel Text for Carton Label:

Well at

Walgreens NDC 0363-9040-00

WALGREENS PHARMACIST RECOMMENDED≠

NEW

STERILE

Sodium Chloride

Ophthalmic

Solution USP, 5%

Hypertonicity Eye Drops

0.5 FL OZ (15 mL)

Compare to Muro 128®

active ingredient#

Sodium Chloride

Sodium Chloride SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0363-9040
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
HYPROMELLOSES
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:0363-9040-00 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-02-12


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