REFRESH CELLUVISC- carboxymethylcellulose sodium gel 
Allergan, Inc.

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REFRESH® CELLUVISC® 
Drug Facts

Active ingredient

Carboxymethylcellulose sodium 1%

Purpose

Eye lubricant

Uses

Warnings

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

Inactive ingredients

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

Questions or comments?

1.800.678.1605

refreshbrand.com

v1.0DFL4554

PRINCIPAL DISPLAY PANEL

NDC 0023-4554-30
Preservative-free 
Refresh® 
Celluvisc® 
Lubricant Eye Gel 
EXTRA-STRENGTH GEL 
Soothes & Comforts
Dry, Irritated Eyes30 Single-Use Containers
0.01 fl oz (0.4 mL) each Sterile 

PRINCIPAL DISPLAY PANEL
NDC 0023-4554-30 
Preservative-free 
Refresh® 
Celluvisc® 
Lubricant Eye Gel 
EXTRA-STRENGTH GEL 
Soothes & Comforts
Dry, Irritated Eyes30 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 AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0023-4554-055 in 1 CARTON10/04/1989
10.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2NDC:0023-4554-3030 in 1 CARTON10/04/1989
20.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01810/04/1989
Labeler - Allergan, Inc. (144796497)

Revised: 8/2022
Document Id: 359e69ff-fe54-4933-8df2-92be6662fc1f
Set id: b32ed9e8-d091-4f16-b416-5a62cdfee49a
Version: 9
Effective Time: 20220826
 
Allergan, Inc.