What is NDC 70000-0089?

70000-0089 is the product NDC for Dry Eye Relief (carboxymethylcellulose sodium), Carboxymethylcellulose sodium, Unspecified 10 mg/mL gel, listed with the FDA by CARDINAL HEALTH 110, LLC. DBA LEADER. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Dry Eye Relief (Carboxymethylcellulose sodium).

What is the active ingredient?

Carboxymethylcellulose sodium, Unspecified.

CARDINAL HEALTH 110, LLC. DBA LEADER, NDC labeler code 70000. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Dry Eye Relief?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Dry Eye Relief NDC 70000-0089 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70000-0089Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70000-0089Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
70000-0089-1	7000000890170000008901	1 BOTTLE, DROPPER in 1 CARTON (70000-0089-1) / 15 mL in 1 BOTTLE, DROPPERMarketed from Mar 9, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Dry Eye Relief
Generic name (nonproprietary): carboxymethylcellulose sodium
Active ingredients: Carboxymethylcellulose sodium, Unspecified — 10 mg/mL
Dosage form: Gel
Route: Ophthalmic
Labeler: CARDINAL HEALTH 110, LLC. DBA LEADERNDC labeler code 70000
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M 018
Marketing start: Mar 9, 2021
Marketing end: Nov 30, 2026
Identifiers: Product ID 70000-0089_b2fd3f1c-69bb-4c0c-9a11-1c135377045cSPL ID b2fd3f1c-69bb-4c0c-9a11-1c135377045cSPL set ID bd262028-32e9-052d-e053-2a95a90a5303RxCUI 579907UNII K679OBS311

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470000008901 followed by a unit qualifier and the quantity

Package 70000-0089-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Sep 12, 2025.

Indications (excerpt from the label)

Uses • For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun. • for used as a protectant against further irritation or to relieve dryness of the eye.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70000-0089

What is NDC 70000-0089?: 70000-0089 is the product NDC for Dry Eye Relief (carboxymethylcellulose sodium), Carboxymethylcellulose sodium, Unspecified 10 mg/mL gel, listed with the FDA by CARDINAL HEALTH 110, LLC. DBA LEADER. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Dry Eye Relief (Carboxymethylcellulose sodium).
What is the active ingredient?: Carboxymethylcellulose sodium, Unspecified.
Who is the labeler?: CARDINAL HEALTH 110, LLC. DBA LEADER, NDC labeler code 70000. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dry Eye Relief?: 1 other product NDC are listed under this name. See all Dry Eye Relief NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Dry Eye Relief NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Dry eye reliefpolyethylene glycol and propylene glycol	Polyethylene glycol 400 4 mg/mL; Propylene glycol 3 mg/mL	GelOphthalmic	CARDINAL HEALTH 110, LLC. DBA LEADER	70000-0088	70000-0088-01

Other NDCs under M 018

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under M 018
Product	Strength	Form · route	Labeler	Product NDC
Walgreens Eye Drops Maximum Redness Relief 15mLglycerin, naphazoline hci	Naphazoline hydrochloride .03 g/100mL; Glycerin .5 g/100mL	Solution/ dropsOphthalmic	Walgreen Company	0363-4546
Vista Gonio Eye Lubricanthypromellose ophthalmic solution	Hypromellose 2208 (100 mpa.s) 25 mg/15mL	SolutionOphthalmic	Red Wedding LLC	77790-022
Capasil Pain Relievingmenthol, methyl salicylate	Methyl salicylate 100 mg/mL; Menthol 20 mg/mL	CreamTopical	PureTek Corporation	59088-434
Rugby Eye Washwater, purified	Water 99.05 g/100mL	SolutionOphthalmic	A-S Medication Solutions	50090-7440
DG Original Eye Dropstetrahydrozoline hcl	Tetrahydrozoline hydrochloride .05 g/100mL	SolutionOphthalmic	Dolgencorp LLC	55910-363
TopCare Health Lubricant Eye Dropscarboxymethylcellulose sodium	Carboxymethylcellulose sodium .5 g/100mL	Solution/ dropsOphthalmic	Topcare Associates LLC	76162-089
VitaPhyte Lubricating Eye Dropslubricating eye drops	Carboxymethylcellulose sodium 5 mg/mL; Glycerin 3 mg/mL	SolutionOphthalmic	Guangzhou Liyan Cosmetics Technology Co., Ltd.	87770-008
VISTA Hypromellose Dry Eye Reliefhypromellose	Hypromellose 2910 (50 mpa.s) .3 g/mL	GelOphthalmic	Red Wedding LLC	77790-002
EyS Eye Washwater	Water 14.85 mL/15mL	SolutionOphthalmic	Eyes-Plus LLC	57349-220
DG Health Advanced Relief Eye Dropsdextran 70, polyethylene glycol 400, povidone, tetrahydrozoline hcl	Povidone, Unspecified 1 g/100mL + 3 more ingredients	SolutionOphthalmic	Dolgencorp LLC	55910-361
Fendall 2000 Pure Flowpurified water	Water 98.6 L/100L	LiquidOphthalmic	Honeywell Safety Products USA, Inc.	0498-0631
VISTA MEIBO TEARS Propylene Glycol 0.6% w/v Advanced Dry Eye Relief Lubricating Drops 10 mlpropylene glycol	Propylene glycol .6 g/100mL	LiquidOphthalmic	Red Wedding LLC	77790-003
VitaPhyte Lubricant Eye Dropslubricant eye drops	Carboxymethylcellulose sodium 5 mg/mL; Glycerin 3 mg/mL	SolutionOphthalmic	Guangzhou Liyan Cosmetics Technology Co., Ltd.	87770-020
DG Health Dry Eye Reliefglycerin, hypromellose, polypropylene glycol 400	Polyethylene glycol 400 1 g/100mL + 2 more ingredients	SolutionOphthalmic	Dolgencorp LLC	55910-362
Optaseglycerin	Glycerin 2 mg/mL	Solution/ dropsOphthalmic	Scope Health Inc	72972-002
Rippleglycerin, povidone	Glycerin .63 g/100mL; Povidone .25 g/100mL	Solution/ dropsOphthalmic	CorneaCare Inc	82875-003
Salinenasal	Sodium chloride 6.5 mg/mL	SprayNasal	GERI-CARE PHARMACEUTICAL CORP	57896-333
Signature Care Lubricant Eye Dropscarboxymethylcellulose sodium	Carboxymethylcellulose sodium .5 g/100mL	Solution/ dropsOphthalmic	Better Living Brands LLC	21130-705
Optaseglycerin	Glycerin 1 mg/mL	SprayOphthalmic	Scope Health Inc	72972-001
Discount Drug Mart Eye Drops Multi-Symptom Reliefpolyethylene glycol 400, tetrahydrozoline hcl, zinc sulfate	Zinc sulfate .25 g/100mL + 2 more ingredients	Solution/ dropsOphthalmic	Discount Drug Mart, Inc.	53943-490

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Dry Eye Relief (Carboxymethylcellulose sodium) NDC 70000-0089

NDC codes

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About NDC 70000-0089

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About NDC 70000-0089

Related NDCs: other Dry Eye Relief products

Other NDCs under M 018