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

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Sodium Chloride Hypertonicity

Major Pharmaceuticals

Sodium Chloride Hypertonicity Ophthalmic Ointment Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Sodium chloride, 50 mg (5%)

Purpose

Hypertonicity agent

Sodium Chloride Hypertonicity Uses

temporary relieve of corneal edema

Warnings

Do not use except under the advice and supervision of a doctor

When using this product  

  • it may cause temporary burning and irritation
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after use

Stop use and ask a doctor if

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

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

Directions

  •  pull down the lower lid of the affected eye
  •  apply a small amount (1/4 inch) of ointment to the inside of eyelid
  •  apply every 3 or 4 hours or as directed by a doctor

Sodium Chloride Hypertonicity Other information

  • store at 15° - 30°C (59° - 86°F)
  • keep tightly closed
  • do not freeze

 

Inactive ingredient

lanolin, mineral oil, purified water, white petrolatum

Questions?

Serious side effects associated with use of this product may be reported to 1-800-323-0000

DO NOT ROLL, BEND, TWIST OR FOLD THE TUBE DURING USE AS THIS MAY CAUSE THE TUBE TO TEAR OR CRACK.

Package/Label Principal Display Panel

Sodium Chloride Hypertonicity

0904-5315-38

Sodium Chloride

Hypertonicity

Ophthalmic Ointment, 5%

(Sterile)

FOR USE IN THE EYES ONLY

Net wt. 1/8 oz. (3.5 g)

MAJOR®

Sodium Chloride Hypertonicity

sodium chloride OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0904-5315
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
LANOLIN
water
petrolatum
Mineral Oil

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0904-5315-38 3.5 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-01-01


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