Dry Eye Relief

Manufacturer
CARDINAL HEALTH 110, LLC. DBA LEADER
Effective date
2025-09-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:14:29

Key Label Information#

Active Ingredients And Purpose

Active ingredient

Carboxymethylcellulose sodium 1%

Purpose

Eye lubricant

Warnings

Warnings

• For external use only. • To avoid contamination, do not touch tip of container to any surface. Replace cap after using. • If solution changes color or becomes cloudy, do not use.

Directions And Dosage

Directions

Instill 1 or 2 drops in the affected eye(s) as needed.

Other Label Information

Inactive ingredients

Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; stabilized oxychloro complex; sodium borate; and sodium chloride, May Contain Hydrochloric Acid and /or Sodium hydroxide to adjust PH.

Principal Display Panel

LEADER® NDC 70000-0089-1 Sterile Dry Eye Relief Carboxymethylcellulose Sodium, 1% Eye Lubricant Restores Moisture in Eyes 0.5 FL OZ (15 mL)

Principal Display Panel

LEADER® NDC 70000-0089-1 Sterile Dry Eye Relief Carboxymethylcellulose Sodium, 1% Eye Lubricant Restores Moisture in Eyes Actual Bottle Size on Side Panel COMPARE TO REFRESH LIQUIGEL® LUBRICANT EYE GEL active ingredient* 100% Money Back Guarantee 0.5 FL OZ (15 mL)

Label Images#

c607e857-ab5c-cf66-e053-2a95a90aee36-01
c607e857-ab5c-cf66-e053-2a95a90aee36-01
c607e857-ab5c-cf66-e053-2a95a90aee36-00
c607e857-ab5c-cf66-e053-2a95a90aee36-00

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
579907carboxymethylcellulose sodium 1 % Ophthalmic GelPSN3
579907carboxymethylcellulose sodium 0.01 MG/MG Ophthalmic GelSCD3
579907carboxymethylcellulose sodium 1 % Ophthalmic GelSY3

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
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
70000-0089-12025-09-22C16284748780-11030e365-1670-111a-e063-dadaa90a10e2Sterile Dry Eye Relief
70000-0089-12024-01-30C16284748780-11030e365-1670-111a-e063-dadaa90a10e2Sterile Dry Eye Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70000-0089-1Dry Eye Relief1 in 1 CARTONGEL13
70000-0089-1Dry Eye Relief15 mL in 1 BOTTLE, DROPPERGEL153

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70000-0089-1ML - Milliliter70000-0089bfff43f6-6ed9-4f77-bc84-4c2f6991bb0312022-02-07

Products#

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70000-008970000-0089-1

Ingredients#

Complete SPL Sections#

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Carboxymethylcellulose sodium 1%

Purpose

OTC - PURPOSE SECTION

Eye lubricant

Warnings

WARNINGS SECTION

• For external use only. • To avoid contamination, do not touch tip of container to any surface. Replace cap after using. • If solution changes color or becomes cloudy, do not use.

Directions

DOSAGE & ADMINISTRATION SECTION

Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

SPL UNCLASSIFIED SECTION

▪ Use only if imprinted tape seals on top and bottom flaps are intact and clearly legible. ▪ Use before expiration date marked on container. ▪ Discard 90 days after opening. ▪ Store at 59°-86°F (15°-30°C). ▪ RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; stabilized oxychloro complex; sodium borate; and sodium chloride, May Contain Hydrochloric Acid and /or Sodium hydroxide to adjust PH.

.

SPL UNCLASSIFIED SECTION

TAMPER EVIDENT Do not use if tape seals on carton top and bottom flaps are damaged or missing. *This product is not manufactured or distributed by Allergan, Inc., owner of the registered trademark Refresh Liquigel® Lubricant Eye Ge;. DISTRIBUTED BY CARDINAL HEALTH DUBLIN, OHIO 43017 www.myleader.com 1-800-200-6313 Made in India 100% Money Back Guarantee Return to place of purchase if not satisfied. Code: MH/DRUGS/28-KD/283 CIN 5698360 REV. 2/21

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LEADER® NDC 70000-0089-1 Sterile Dry Eye Relief Carboxymethylcellulose Sodium, 1% Eye Lubricant Restores Moisture in Eyes 0.5 FL OZ (15 mL)

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LEADER® NDC 70000-0089-1 Sterile Dry Eye Relief Carboxymethylcellulose Sodium, 1% Eye Lubricant Restores Moisture in Eyes Actual Bottle Size on Side Panel COMPARE TO REFRESH LIQUIGEL® LUBRICANT EYE GEL active ingredient* 100% Money Back Guarantee 0.5 FL OZ (15 mL)

Source Document#

Source XML