REFRESH CELLUVISC description, usages, side effects, indications, overdosage, supplying and lots more!

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REFRESH CELLUVISC

Allergan, Inc.

REFRESH CELLUVISC Lubricant Eye Drops


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Carboxymethylcellulose sodium 1%

Purpose

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.
  • If solution changes color or becomes cloudy, do not use.

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.

Other information

  • Use only if single-use container is intact.
  • REFRESH® CELLUVISC® may cause temporary blurring due to its viscosity.
  • Store at 59°-86°F (15°-30°C).
  • Use before expiration date marked on container.
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Calcium chloride; potassium chloride; purified water; sodium chloride; and sodium lactate.

Questions or comments?

1.800.433.8871
refreshbrand.com

NDC 0023-4554-30

Preservative-free

Refresh®
Celluvisc®
Lubricant Eye Gel

Soothing Gel

Long-lasting relief
for dry eyes in a
soothing gel formula

30 Single-Use Containers
0.01 fl oz (0.4 mL) each Sterile

REFRESH CELLUVISC

carboxymethylcellulose sodium GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0023-4554
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARBOXYMETHYLCELLULOSE SODIUM 10 mg

Inactive Ingredients

Ingredient Name Strength
calcium chloride
potassium chloride
water
SODIUM CHLORIDE
sodium lactate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 0.4 in 1 VIAL, SINGLE-USE
2 0.4 in 1 VIAL, SINGLE-USE
3 NDC:0023-4554-30 30 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 1989-10-04


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Be sure to consult your doctor before taking any medication!
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