FDA.reportPublic FDA data

REFRESH ® CELLUVISC ® Drug Facts

Manufacturer
Allergan, Inc.
Effective date
2026-06-05
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
daily-update
Hydrated at
2026-06-18 05:10:09

Label at a glance#

ProductREFRESH CELLUVISC
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure9 sections

Indications and 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.

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Carboxymethylcellulose sodium 1%

Purpose

OTC - PURPOSE SECTION

Eye lubricant

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

  • 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

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY INFORMATION

  • Use only if single-use container is intact.
  • REFRESH® CELLUVISC® may cause temporary blurring due to its viscosity.
  • Store at 59°-77°F (15°-25°C).
  • Use before expiration date marked on container.
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions or comments?

OTC - QUESTIONS SECTION

1.800.678.1605

refresheyedrops.com

v2.0DFL4554

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0023-4554-30
PRESERVATIVE-FREE
Refresh ® 
CELLUVISC ® 
Lubricant Eye Gel
Soothes & Comforts
Dry, Irritated Eyes
30 Vials 0.01 fl oz (0.4 mL) each Sterile

PRINCIPAL DISPLAY PANEL NDC 0023-4554-30 PRESERVATIVE-FREE Refresh ® CELLUVISC ® Lubricant Eye Gel Soothes & Comforts Dry, Irritated Eyes 30 Vials 0.01 fl oz (0.4 mL) each SterilePRINCIPAL DISPLAY PANEL NDC 0023-4554-30 PRESERVATIVE-FREE Refresh ® CELLUVISC ® Lubricant Eye Gel Soothes & Comforts Dry, Irritated Eyes 30 Vials 0.01 fl oz (0.4 mL) each Sterile

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0023-4554-30EA - Each0023-45540649df12-88d2-4290-a201-b12da7c5ec9512012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
carboxymethylcellulose sodiumACTIVE INGREDIENTK679OBS3114
carboxymethylcelluloseACTIVE MOIETY05JZI7B19X4
calcium chlorideINACTIVE INGREDIENTM4I0D6VV5M4
potassium chlorideINACTIVE INGREDIENT660YQ98I104
sodium chlorideINACTIVE INGREDIENT451W47IQ8X4
sodium lactateINACTIVE INGREDIENTTU7HW0W0QT4
waterINACTIVE INGREDIENT059QF0KO0R4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0023-45540023-4554-05, 0023-4554-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311ACTIB
CALCIUM CHLORIDEM4I0D6VV5MIACT
POTASSIUM CHLORIDE660YQ98I10IACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM LACTATETU7HW0W0QTIACT

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
92022-08-26full-release2026-06-01 00:08:13

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 21 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
sodium lactateSODIUM LACTATETU7HW0W0QTGEL / TOPICAL4 mgExact identifier — unii+dosage form
3 equally ranked IID candidates
potassium chloridePOTASSIUM CHLORIDE660YQ98I10SOLUTION/ DROPS / OPHTHALMIC0.14 %w/vExact identifier — unii+route
9 equally ranked IID candidates
potassium chloridePOTASSIUM CHLORIDE660YQ98I10SOLUTION/ DROPS / OPHTHALMIC0.14 %w/vExact identifier — unii+route
9 equally ranked IID candidates
potassium chloridePOTASSIUM CHLORIDE660YQ98I10SOLUTION / OPHTHALMIC0.22 %w/vExact identifier — unii+route
9 equally ranked IID candidates
calcium chlorideCALCIUM CHLORIDEM4I0D6VV5MSOLUTION/ DROPS / OPHTHALMIC0.02 %w/vExact identifier — unii+route
6 equally ranked IID candidates
sodium lactateSODIUM LACTATETU7HW0W0QTGEL / TOPICAL4 mgExact identifier — unii+dosage form
3 equally ranked IID candidates
potassium chloridePOTASSIUM CHLORIDE660YQ98I10SUSPENSION / OPHTHALMIC0.03 %w/wExact identifier — unii+route
9 equally ranked IID candidates
potassium chloridePOTASSIUM CHLORIDE660YQ98I10SOLUTION / OPHTHALMIC0.22 %w/vExact identifier — unii+route
9 equally ranked IID candidates
sodium chlorideSODIUM CHLORIDE451W47IQ8XGEL / OPHTHALMIC0.9 %w/vExact identifier — unii+route+dosage form
3 equally ranked IID candidates
calcium chlorideCALCIUM CHLORIDEM4I0D6VV5MSOLUTION / OPHTHALMIC1 mgExact identifier — unii+route
6 equally ranked IID candidates
sodium chlorideSODIUM CHLORIDE451W47IQ8XGEL / OPHTHALMIC0.9 %w/vExact identifier — unii+route+dosage form
3 equally ranked IID candidates
sodium lactateSODIUM LACTATETU7HW0W0QTGEL / TOPICAL4 mgExact identifier — unii+dosage form
3 equally ranked IID candidates
potassium chloridePOTASSIUM CHLORIDE660YQ98I10SUSPENSION / OPHTHALMIC0.03 %w/wExact identifier — unii+route
9 equally ranked IID candidates
calcium chlorideCALCIUM CHLORIDEM4I0D6VV5MSOLUTION/ DROPS / OPHTHALMIC0.02 %w/vExact identifier — unii+route
6 equally ranked IID candidates
calcium chlorideCALCIUM CHLORIDEM4I0D6VV5MSOLUTION / OPHTHALMIC1 mgExact identifier — unii+route
6 equally ranked IID candidates
potassium chloridePOTASSIUM CHLORIDE660YQ98I10SOLUTION / OPHTHALMIC0.22 %w/vExact identifier — unii+route
9 equally ranked IID candidates
sodium chlorideSODIUM CHLORIDE451W47IQ8XGEL / OPHTHALMIC0.9 %w/vExact identifier — unii+route+dosage form
3 equally ranked IID candidates
potassium chloridePOTASSIUM CHLORIDE660YQ98I10SOLUTION/ DROPS / OPHTHALMIC0.14 %w/vExact identifier — unii+route
9 equally ranked IID candidates
calcium chlorideCALCIUM CHLORIDEM4I0D6VV5MSOLUTION/ DROPS / OPHTHALMIC0.02 %w/vExact identifier — unii+route
6 equally ranked IID candidates
calcium chlorideCALCIUM CHLORIDEM4I0D6VV5MSOLUTION / OPHTHALMIC1 mgExact identifier — unii+route
6 equally ranked IID candidates
potassium chloridePOTASSIUM CHLORIDE660YQ98I10SUSPENSION / OPHTHALMIC0.03 %w/wExact identifier — unii+route
9 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
REFRESH CELLUVISCCARBOXYMETHYLCELLULOSE SODIUMAllergan, Inc.b32ed9e8-d091-4f16-b416-5a62cdfee49a2026-06-05WarningsExact identifier
ndc (package): 0023-4554-30
ndc (package): 0023-4554-05
ndc (product): 0023-4554
ndc11 (package): 00023455405
ndc11 (package): 00023455430
spl id: d557bb82-b2a0-4be8-80a2-196c328bff3f
spl set id: b32ed9e8-d091-4f16-b416-5a62cdfee49a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.