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 Solution Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Sodium chloride 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
  • if solution changes color or becomes cloudy

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

  •  instill 1 or 2 drops in the affected eye(s) every 3 or 4 hours, or as directed by a physician.

Sodium Chloride Hypertonicity Other information

  • store upright at 15° - 30°C (59° - 86°F)
  • keep tightly closed

 

Inactive ingredient

boric acid, hypromellose, propylene glycol, purified water, sodium borate. Sodium hydroxide ad/or hydrochloric acid may be added to adjust pH. PRESERVATIVE ADDED: methylparaben 0.023%, propylparaben 0.01%

Questions?

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

Package/Label Principal Display Panel

Sodium Chloride Hypertonicity

NDC 0904-5314-35

Sodium Chloride Hypertonicity Ophthalmic Solution USP, 5%

(Sterile)

For temporary relief of Corneal Edema

1/2 fl oz (15mL)

MAJOR®

Sodium Chloride Hypertonicity

sodium chloride SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0904-5314
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 2208 (100 MPA.S)
propylene glycol
water
SODIUM BORATE
METHYLPARABEN
PROPYLPARABEN
SODIUM HYDROXIDE
HYDROCHLORIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE
2 NDC:0904-5314-35 1 in 1 CARTON

Marketing Information

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


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