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
  • do not use if cap is dislodged from tube
  • 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 occur
  • continued redress or irritation of the eye
  • the condition worsens or persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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 20° to 25° C (68° to 77°F) [see USP Controlled Room Temperature].
  • store away from heat
  • protect from freezing
  • keep tightly closed
  • see crimp for Lot Number and Expiration Date
  • RETAIN THIS CARTON FOR FUTURE REFERENCE

Inactive ingredients

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

Questions or comments?

1-800-932-5676

Principal Display Panel Text for Container Label:

STERILE Well at

Sodium Chloride Walgreens

Ophthalmic Ointment NDC 0363-9050-00

USP, 5% NET WT 3.5 g (1/8 oz.)

Hypertonicity Eye Ointment

FOR OPHTHALMIC USE ONLY

Principal Display Panel Text for Carton Label:

STERILE Well at

Walgreens

WALGREENS PHARMACIST RECOMMENDED≠

Sodium Chloride

Ophthalmic Ointment NDC 0363-9050-00

USP, 5%

Hypertonicity Eye Ointment

Compare to Muro 128®

NET WT 3.5 g (1/8 OZ) Ointment active ingredient#

Sodium Chloride

Sodium Chloride OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0363-9050
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:0363-9050-00 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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