FDA.reportPublic FDA data

Lubricant Eye Drops

Manufacturer
Oliver Landon Intl Inc.
Effective date
2020-11-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:35:40

Label at a glance#

ProductLubricant Eye Drops
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure11 sections

Storage and handling

Other information use before expiration date marked on container. store at 59°-86°F (15°-33°C) RETAIN THIS CARD FOR FUTURE REFERENCE. Use only if single-use container is intact.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Carboxymethylcellulose sodium 0.5%

OTC - PURPOSE SECTION

Purpose

Eye Lubricant

INDICATIONS & USAGE SECTION

Uses

  • for the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to wind or sun.
  • protects against further irritation.

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use if solution changes color or becomes cloudy

OTC - WHEN USING SECTION

When using this product

  • do not touch tip of container to any surface to avoid contamination.
  • do not reuse. Once opened, discard.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • you experience eye pain, changes in vision, continued redness or irritation of the eye
  • condition worsens or persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

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

*If used for post-operative dryness and discomfort, follow your eye doctor’s instructions.

STORAGE AND HANDLING SECTION

Other information

  • use before expiration date marked on container.
  • store at 59°-86°F (15°-33°C)

RETAIN THIS CARD FOR FUTURE REFERENCE.

Use only if single-use container is intact.

INACTIVE INGREDIENT SECTION

Inactive ingredients Calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride and sodium lactate.

May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

OTC - QUESTIONS SECTION

Questions & Comments? 1 (800) 839-5929

SPL UNCLASSIFIED SECTION

Manufactured for: Oliver Landon Intl. Inc.

The Grove, 21 Pine Road

Belleville, St. Michael, BARBADOS BB11113

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lubricant Eye Drops
0.4 ml (0.014 fl oz) per vial

Lubricant Eye Drops vial labelLubricant Eye Drops vial label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionPSN2
1188426carboxymethylcellulose sodium 5 MG/ML Ophthalmic SolutionSCD2
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionSY2
1188426carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic SolutionSY2

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59276-905-052024-01-30C16284748780-11030e365-6d7f-111a-e063-dadaa90a10e2Lubricant Eye Drops

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59276-905-05Lubricant Eye Drops0.4 mL in 1 VIAL, SINGLE-USESOLUTION/ DROPS0.42
59276-905-05Lubricant Eye Drops5 in 1 CELLO PACKSOLUTION/ DROPS52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59276-905LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [OLIVER LANDON INTL INC.]2Legacy NDC, 2 package rows20201221_ec3160ac-a2d1-4132-a75a-4180b4bafdf3.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59276-90559276-905-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALCIUM CHLORIDEM4I0D6VV5MIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
POTASSIUM CHLORIDE660YQ98I10IACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM LACTATETU7HW0W0QTIACT
HYDROCHLORIC ACIDQTT17582CBIACT
SODIUM HYDROXIDE55X04QC32IIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311ACTIB

Source Document#

Source XML

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
b4e07cf0-5f4c-bcaf-e053-2995a90aee25ec3160ac-a2d1-4132-a75a-4180b4bafdf32020-11-24WarningsExact identifier
spl id: b4e07cf0-5f4c-bcaf-e053-2995a90aee25
spl set id: ec3160ac-a2d1-4132-a75a-4180b4bafdf3

Reported adverse events (FAERS/openFDA)#

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