REFRESH CELLUVISC- carboxymethylcellulose sodium gel

REFRESH CELLUVISC by

Drug Labeling and Warnings

REFRESH CELLUVISC by is a Otc medication manufactured, distributed, or labeled by Allergan, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.
  
• 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

PRINCIPAL DISPLAY PANEL

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 

INGREDIENTS AND APPEARANCE

REFRESH CELLUVISC 
carboxymethylcellulose sodium gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0023-4554
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LACTATE (UNII: TU7HW0W0QT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0023-4554-05	5 in 1 CARTON	10/04/1989
1		0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2	NDC: 0023-4554-30	30 in 1 CARTON	10/04/1989
2		0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part349	10/04/1989

Labeler - Allergan, Inc. (144796497)