Dry Eye Relief

Product NDC: 70000-0089
11-digit product format: 700000089
Labeler code: 70000
Product ID: 70000-0089_b2fd3f1c-69bb-4c0c-9a11-1c135377045c
Type: HUMAN OTC DRUG
Nonproprietary name: Carboxymethylcellulose sodium
Dosage form: GEL
Route: OPHTHALMIC
Labeler: CARDINAL HEALTH 110, LLC. DBA LEADER
Application: M018
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-03-09
Marketing end: 2026-11-30
Substance: CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Active strength: 10 mg/mL
NDC exclude flag: No
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 28 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	70000-0089-1	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	70000-0089-1	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	70000-0089-1	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	70000-0089-1	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	70000-0089-1	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	70000-0089-1	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	70000-0089-1	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	70000-0089-1	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	70000-0089-1	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	70000-0089-1	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	70000-0089-1	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	70000-0089-1	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	70000-0089-1	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	70000-0089-1	`1332a3947898…`	`d4bfe170f9cd…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Dry Eye Relief

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED	10 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
K679OBS311	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
579907	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
bd262028-32e9-052d-e053-2a95a90a5303	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
9e37788c-b1bf-42ae-aac9-b60601606144	Product name	8	20260122
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2	Product name	5	20250304
1527ac37-808d-43be-a63e-74e1258dbe46	Product name	9	20250219
bed0530e-f939-4541-956b-6928a2f6404f	Product name	1	20241008
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	6	20240814
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5	Product name	8	20230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
0ec3537a-6c9b-432a-896c-b9ea8723049a	Product name	9	20200701
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
7916de40-e296-41f0-b811-6d0df1a33e2c	Product name	9	20180627
cefa60e2-a5b5-493e-9c54-24735b7dc509	Product name	2	20171212
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
5668b646-cd56-c3c7-bdea-3f6b1a8840db	Product name	1	20140508
810ab97e-f109-f41c-7c83-6a652a9cbf43	Product name	1	20140508
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2dd	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70000-0089-1	2025-09-22	C162847	48780-1	1030e365-1670-111a-e063-dadaa90a10e2	Sterile Dry Eye Relief
70000-0089-1	2024-01-30	C162847	48780-1	1030e365-1670-111a-e063-dadaa90a10e2	Sterile Dry Eye Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70000-0089-1	Dry Eye Relief	1 in 1 CARTON	GEL	1		3
70000-0089-1	Dry Eye Relief	15 mL in 1 BOTTLE, DROPPER	GEL	15		3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70000-0089-1	ML - Milliliter	70000-0089	bfff43f6-6ed9-4f77-bc84-4c2f6991bb03	1	2022-02-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70000-0089	DRY EYE RELIEF (CARBOXYMETHYLCELLULOSE SODIUM) GEL [CARDINAL HEALTH, 110 DBA LEADER]	2	Current NDC, Legacy NDC, 2 package rows	20210701_bd262028-32e9-052d-e053-2a95a90a5303.zip

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 12 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Quality Choice Lubricant Eye Drops Long Lasting	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Chain Drug Marketing Assoc., Inc.	0cd91c45-88a2-f88c-e063-6294a90ad127	2025-12-30	Warnings	Exact identifier application number: M018
Quality Choice Eye Wash	WATER	Chain Drug Marketing Assoc., Inc.	1fb8a109-351b-7039-e063-6394a90a7311	2025-12-30	Warnings	Exact identifier application number: M018
Rite Aid Eye Wash	PURIFIED WATER	Rite Aid	28a18e04-d735-a511-e063-6394a90af6bb	2025-12-30	Warnings	Exact identifier application number: M018
Preferred Plus Pharmacy Redness Relief Eye Drops	TETRAHYDROZOLINE HCL	Kinray	9ffd67c4-b5c1-d587-e053-2a95a90ae3d0	2025-12-30	Warnings	Exact identifier application number: M018
Leader Lubricant Eye Drops Soothing Relief	CARBOXYMETHYLCELLULOSE SODIUM	LEADER/Cardinal Health 110, Inc.	218629d4-2704-a503-e063-6294a90a3953	2025-12-30	Warnings	Exact identifier application number: M018
Foster and Thrive Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Strategic Sourcing Services LLC	fb85ebc0-1570-972b-e053-6294a90a3dc4	2025-12-30	Warnings	Exact identifier application number: M018
Archies Dry Eye Relief	POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL	Archie's Remedies	07da099b-6b7f-984d-e063-6294a90a12ac	2025-12-30	Warnings	Exact identifier application number: M018
Equate Optimal Hydration Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN	Walmart, Inc.	151b9723-5d5e-ac2b-e063-6294a90af073	2025-12-30	Warnings	Exact identifier application number: M018
Equate Nighttime Relief Lubricant	LIGHT MINERAL OIL, WHITE PETROLATUM	Walmart Inc.	152171db-2f2a-9d36-e063-6394a90a7225	2025-12-30	Warnings	Exact identifier application number: M018
Equate Moisturizing Comfort Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Walmart Inc.	152028bd-0429-720a-e063-6294a90a1465	2025-12-30	Warnings	Exact identifier application number: M018
Equaline Multi-Symptom Eye Drops	POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE	United Natural Foods, Inc.	fe467606-6d66-b695-e053-6294a90aab5d	2025-12-30	Warnings	Exact identifier application number: M018
OCUFRESH	WATER	Optics Laboratory Inc.	b8e477a9-66b9-496b-92fb-3d4bbd7b36b5	2025-12-29	Warnings	Exact identifier application number: M018
Kollourion Eyesalve Eyewash	PURIFIED WATER 98.3%	Miracle Eye Pharmaceuticals	b56d2ab9-169b-b490-e053-2a95a90a80b3	2025-12-28	Warnings	Exact identifier application number: M018
Equate Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN	Hanlim	46851e7c-8910-6456-e063-6394a90abafb	2025-12-22	Warnings	Exact identifier application number: M018
Equate Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Hanlim	46854996-a0b9-46b4-e063-6294a90aa433	2025-12-22	Warnings	Exact identifier application number: M018
Equate Nighttime Relief Lubricant	LIGHT MINERAL OIL, WHITE PETROLATUM	Hanlim Pharm Co. LTD	468559a0-9586-9982-e063-6394a90af466	2025-12-22	Warnings	Exact identifier application number: M018
Redness and Dry Eye Relief	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	KC Pharmaceuticals, Inc	4682f68d-6bdd-d860-e063-6394a90a2b52	2025-12-21	Warnings	Exact identifier application number: M018
Original Redness Reliever	TETRAHYDROLIZINE HCL	KC Pharmaceuticals	4683b850-b0fc-5093-e063-6294a90aef44	2025-12-21	Warnings	Exact identifier application number: M018
Equate Nighttime Relief Lubricant	LIGHT MINERAL OIL, WHITE PETROLATUM	Walmart	4449a55b-2cd4-0cb9-e063-6294a90aafbc	2025-12-20	Warnings	Exact identifier application number: M018
Equate Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	Walmart	44494842-e38d-617c-e063-6294a90afaf8	2025-12-20	Warnings	Exact identifier application number: M018

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
579907	carboxymethylcellulose sodium 1 % Ophthalmic Gel	PSN	bd262028-32e9-052d-e053-2a95a90a5303	3
579907	carboxymethylcellulose sodium 0.01 MG/MG Ophthalmic Gel	SCD	bd262028-32e9-052d-e053-2a95a90a5303	3
579907	carboxymethylcellulose sodium 1 % Ophthalmic Gel	SY	bd262028-32e9-052d-e053-2a95a90a5303	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
70000-0089-1	70000008901	1 BOTTLE, DROPPER in 1 CARTON (70000-0089-1) / 15 mL in 1 BOTTLE, DROPPER	2021-03-09	2026-11-30	No	No	Current