Carboxymethylcellulose sodium description, usages, side effects, indications, overdosage, supplying and lots more!

Carboxymethylcellulose sodium

PROMED EXPORTS PRIVATE LIMITED

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

Carboxymethylcellulose sodium (CMC) 0.5% ............... Eye lubricant

USES

  • For the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to wind or sun.
  • May be used as a protectant against further irritation.

WARNINGS

  • For external use only.
  • To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.
  • Do not touch unit-dose tip to eye.
  • Do not use if solution changes color or becomes cloudy.

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 REACH OF CHILDREN

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

DIRECTIONS

To open, TWIST AND PULL TAB TO REMOVE. Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

If used for post-operative (e.g. LASIK) dryness and discomfort, follow your eye doctor’s instructions.

OTHER INFORMATION

  • Use only if single-use container is intact.
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

INACTIVE INGREDIENTS

Calcium chloride; magnesium chloride; potassium chloride; purified water; sodium chloride; and sodium lactate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL- 30 Sterile Single Use Containers


CARBOXYMETHYLCELLULOSE SODIUM (CMC) 0.5%
LUBRICANT EYE DROPS


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL- 30 Sterile Single Use Containers

Carboxymethylcellulose sodium

Carboxymethylcellulose sodium SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49668-001
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARBOXYMETHYLCELLULOSE SODIUM 5 mg

Inactive Ingredients

Ingredient Name Strength
calcium chloride
MAGNESIUM CHLORIDE
potassium chloride
water
SODIUM CHLORIDE
sodium lactate
HYDROCHLORIC ACID
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.4 in 1 VIAL, SINGLE-DOSE
2 NDC:49668-001-01 30 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2009-10-01


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Be sure to consult your doctor before taking any medication!
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