REFRESH CELLUVISC

Dosage form: gel
Ingredients: carboxymethylcellulose sodium 10mg in 1mL
Labeler: Allergan, Inc.
NDC Code: 0023-4554

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

REFRESH® CELLUVISC® Lubricant Eye Drops

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-4554
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
carboxymethylcellulose sodium (carboxymethylcellulose) carboxymethylcellulose sodium10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
calcium chloride 
potassium chloride 
water 
sodium chloride 
sodium lactate 
Packaging
#Item CodePackage Description
1NDC:0023-4554-055 VIAL, SINGLE-USE in 1 CARTON
10.4 mL in 1 VIAL, SINGLE-USE
2NDC:0023-4554-3030 VIAL, SINGLE-USE in 1 CARTON
20.4 mL in 1 VIAL, SINGLE-USE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34910/04/1989
Labeler - Allergan, Inc. (144796497)
Establishment
NameAddressID/FEIOperations
Allergan, Inc.362898611MANUFACTURE(0023-4554)
Establishment
NameAddressID/FEIOperations
Allergan Pharmaceuticals Ireland219682291MANUFACTURE(0023-4554)

Revised: 11/2011
 
Allergan, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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