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

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Sodium Chloride

HUB Pharmaceuticals

Sodium Chloride 5% Solution USP (Sterile)




FULL PRESCRIBING INFORMATION

Active Ingredien

(each mL contains)

Purpose

Sodium Chloride USP

5% w/v (50mg)

Eye Lubricant

Methylparaben

USP 0.023% w/v

Propylparaben USP 0.01% w/v

Boric Acid, Hypromellose, Propylene Glycol, Sodium Borate, and Water for Injection. Sodium Hydroxide and/or Hydrochloric Acid may be added to adjust pH.

  • To open, twist cap clockwise to puncture sterile seal.
  • Remove cap.
  • Instill 1 or 2 drops in the affected eye(s) every 3 or 4 hours as needed or directed by a doctor.

Instill 1 or 2 drops in the affected eye(s) every 3 or 4 hours as needed or directed by a doctor.

For the temporaty relief of corneal edema.

Purpose

For the temporaty relief of corneal edema.

When using this product:

  • Keep tightly closed.
  • To avoid contamination, do not touch top of container to any surface.
  • Replace cap after using.
  • Do not use except under the advice and supervision of a doctor.
  • If solution changes color or becomes cloudy, do not use.
  • This product may cause temporary burning and irritation on being instilled into the eye.

In case of accidental ingestion, seek professional help or contact a Poision Control Center immediately.

Stop use and ask a doctor if:

  • You experience eye pain, changes in vision, continued redness, or irritation of the eye.
  • The condition worses or persists for more than 72 hours.

DO NOT USE IF IMPRINTED SEAL ON CAP IS TORN, BROKEN, OR MISSING AND IF IMPRINTED DEALS ON TOP AND BOTTOM FLAPS ARE NOT INTACT AND CCOMPLETELY LEGIBLE.

FOR USE IN EYES ONLY.

DO NOT DISCARD BOX. SAVE FOR COMPLETE WARNINGS AND INSTRUCTIONS.

KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN.

Store at room temperature 15°-30°C (59°-86°F).

Sodium Chloride

Sodium Chloride Solution Label

Sodium Chloride

Sodium Chloride SolutionBox

Sodium Chloride

Sodium Chloride SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:17238-625
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
METHYLPARABEN
PROPYLPARABEN
BORIC ACID
HYPROMELLOSES
propylene glycol
SODIUM BORATE
water
SODIUM HYDROXIDE
HYDROCHLORIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, PLASTIC
2 NDC:17238-625-15 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-09-12


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Be sure to consult your doctor before taking any medication!
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