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 temporary relief of corneal edema.

Warnings

  • Do not use this product except under the advice and supervision of a doctor.
  • Do not use if bottom ridge of tube cap is exposed.
  • To avoid contamination, do not touch tip of container to any surface.
  • Replace cap after using.
  • May cause temporary burning and irritation upon application into the eye.

Stop use and ask a doctor if

you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.

Keep out of the reach of children.

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

Questions or comments? 1-800-579-8327

Directions

Apply small amount (one-fourth inch) to the inside of affected eye(s) every 3 to 4 hours, or as directed by a doctor.

Other information

  • Store at controlled room temperature 20° to 25°C (68° to 77°F).
  • Store away from heat.
  • Protect from freezing.
  • Keep tightly closed.
  • See crimp for Control Number and Expiration Date.
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Mineral Oil, Modified Lanolin, Purified Water and White Petrolatum.

Principal Display Panel Text for Container Label:

NDC 59779-303-01

CVS®

pharmacy

Sodium Chloride, USP 5%

Hypertonicity OPHTHALMIC OINTMENT

STERILE NET WT .125 OZ (3.5 g)

Principal Display Panel Text for Carton Label:

CVS® NDC 59779-303-01

Pharmacy Compare to the active

ingredient in MURO 128®*

Sodium Chloride, USP 5%

Hypertonicity OPHTHALMIC OINTMENT

● Temporary relief of corneal edema

NET WT .125 OZ (3.5 g) STERILE

Sodium Chloride

Sodium Chloride OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59779-303
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
Mineral Oil
LANOLIN
water
petrolatum

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 3.5 in 1 TUBE
2 NDC:59779-303-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-02-21


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Be sure to consult your doctor before taking any medication!
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