Systane

Product NDC
0065-0474
11-digit product format
000650474
Labeler code
0065
Product ID
0065-0474_634b9bdb-004a-462e-ba48-1ab306157e02
Type
HUMAN OTC DRUG
Nonproprietary name
hypromellose
Dosage form
GEL
Route
OPHTHALMIC
Labeler
Alcon Laboratories, Inc.
Application
M018
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-12-15
Substance
HYPROMELLOSE 2910 (4000 MPA.S)
Active strength
3 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage0065-04740065-0474-02DDiscontinued by firm2026-10-15

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

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
Systane
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HYPROMELLOSE 2910 (4000 MPA.S)3 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
RN3152OP35Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
310932Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
5f74b161-ae41-d0e2-6ed9-8deca55d2c0fAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0065-0474-01Systane10 g in 1 TUBEGEL109
0065-0474-01Systane1 in 1 CARTONGEL19
0065-0474-02Systane3.5 g in 1 TUBEGEL3.59
0065-0474-02Systane1 in 1 CARTONGEL19

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0065-0474-01GM - Gram0065-0474315f0943-1ba5-4252-9ab2-ff36639f9cb112013-03-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Hypromellose 2910 (4000 Mpa.s)ACTIVE INGREDIENTRN3152OP35SYSTANE (HYPROMELLOSE) GEL [ALCON LABORATORIES, INC.]1
Hypromellose 2910 (4000 Mpa.s)ACTIVE MOIETYRN3152OP35SYSTANE (HYPROMELLOSE) GEL [ALCON LABORATORIES, INC.]1
Carbomer Homopolymer Type C (allyl Pentaerythritol Crosslinked)INACTIVE INGREDIENT4Q93RCW27ESYSTANE (HYPROMELLOSE) GEL [ALCON LABORATORIES, INC.]1
Phosphonic AcidINACTIVE INGREDIENT35V6A8JW8ESYSTANE (HYPROMELLOSE) GEL [ALCON LABORATORIES, INC.]1
Sodium HydroxideINACTIVE INGREDIENT55X04QC32ISYSTANE (HYPROMELLOSE) GEL [ALCON LABORATORIES, INC.]1
Sodium PerborateINACTIVE INGREDIENTY52BK1W96CSYSTANE (HYPROMELLOSE) GEL [ALCON LABORATORIES, INC.]1
SorbitolINACTIVE INGREDIENT506T60A25RSYSTANE (HYPROMELLOSE) GEL [ALCON LABORATORIES, INC.]1
WaterINACTIVE INGREDIENT059QF0KO0RSYSTANE (HYPROMELLOSE) GEL [ALCON LABORATORIES, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0065-0474SYSTANE (HYPROMELLOSE) GEL [ALCON LABORATORIES, INC.]9Current NDC, Legacy NDC, 4 package rows20231216_5f74b161-ae41-d0e2-6ed9-8deca55d2c0f.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 13 of 25 · 494 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Equate Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUM, GLYCERINWalmart443e214b-2680-79a9-e063-6294a90a68ba2025-12-20WarningsExact identifier
application number: M018
Equate Redness and Dry Eye ReliefGLYCERIN, NAPHAZOLINE HYDROCHLORIDEWalmart44155cf8-6fd9-d16f-e063-6394a90ac7312025-12-20WarningsExact identifier
application number: M018
Original Redness RelieverTETRAHYDROLIZINE HCLWalmart4414f768-0c69-d041-e063-6294a90a5bd92025-12-20WarningsExact identifier
application number: M018
Walgreens LubricantPOLYETHYLENE GLYCOL 400, AND PROPYLENE GLYCOLWalgreens21dfe061-4538-2061-e063-6394a90a6e732025-12-19WarningsExact identifier
application number: M018
Artificial TearsGLYCERINGeri-Care Pharmaceuticals, Corp7cc437e3-bad9-59be-e053-2991aa0a1da32025-12-19WarningsExact identifier
application number: M018
Signature Care Eye Drops Redness and Dry Eye ReliefGLYCERIN, NAPHAZOLINE HYDROCHLORIDEBetter Living Brands LLC901f3bbe-e1bb-4e44-879c-711e59813a7f2025-12-19WarningsExact identifier
application number: M018
STYE RELIEF SERUMCARBOXYMETHYLCELLULOSE SODIUM(CMC)Guangzhou Shimei Cosmetics Co., Ltd.45fa7962-b489-4613-e063-6394a90a59b02025-12-15WarningsExact identifier
application number: M018
Gentle Eyes Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUMTRP Company13f99af6-b7d8-a092-e063-6394a90a5daa2025-12-15WarningsExact identifier
application number: M018
Artificial TearsGLYCERINNuCare Pharmaceuticals,Inc.97a3d8e2-b2c0-3f5d-e053-2a95a90ac49d2025-12-15WarningsExact identifier
application number: M018
Eyelash SerumEYELASH SERUMFlexiGo Inc4544adf7-bb24-cb10-e063-6294a90aa4142025-12-06WarningsExact identifier
application number: M018
Redness Reliever, Circle KTETRAHYDROZOLINE HYDROCHLORIDE LIQUIDLil' Drug Store products, Inc.44e95d70-f633-1e4e-e063-6294a90a9f212025-12-01WarningsExact identifier
application number: M018
Splash Pure PFPROPYLENE GLYCOLLABORATORIOS SOPHIA, S.A. DE C.V.40ad7ae5-1f2a-e3b1-e063-6294a90a6f842025-11-26WarningsExact identifier
application number: M018
Eyewash Station Additive ConcentrateCHLORHEXIDINE GLUCONATE AND PROPYLENE GLYCOLNiagara Pharmaceuticals Inc.362a6b6d-862d-4322-87a8-5b3a07fbe1742025-11-24WarningsExact identifier
application number: M018
Rain Daily Hydration and Comfort For Dry EyesGLYCERINRain Eye Drops, LLC31d7c204-fb74-fb28-e063-6294a90ab3302025-11-23WarningsExact identifier
application number: M018
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
application number: M018
Walgreens Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUMWalgreen Companya39864a3-2407-7b7e-e053-2a95a90ab92f2025-11-19WarningsExact identifier
application number: M018
Walgreens Lubricant Eye DropsCARBOXYMETHYLCELLULOSE SODIUMWalgreen Companya39919d5-84db-05df-e053-2995a90ab1d22025-11-19WarningsExact identifier
application number: M018
Sodium ChlorideSODIUM CHLORIDEWalgreen Companyd112a344-33cc-41d3-bae6-492631ebdba72025-11-19WarningsExact identifier
application number: M018
Eyesaline Eyewash ConcentratePURIFIED WATERHoneywell Safety Products USA, Inc.3765c251-eb14-d60f-e063-6294a90a6a4d2025-11-12WarningsExact identifier
application number: M018
Eyesaline Emergency EyewashPURIFIED WATERHoneywell Safety Products USA, Inc.37f244fd-c02f-e66a-e063-6394a90aed812025-11-12WarningsExact identifier
application number: M018

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310932hypromellose 0.3 % Ophthalmic GelPSN5f74b161-ae41-d0e2-6ed9-8deca55d2c0f9
310932hypromellose 0.003 MG/MG Ophthalmic GelSCD5f74b161-ae41-d0e2-6ed9-8deca55d2c0f9
310932hypromellose 0.3 % Ophthalmic GelSY5f74b161-ae41-d0e2-6ed9-8deca55d2c0f9

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0065-0474-01000650474011 TUBE in 1 CARTON (0065-0474-01) / 10 g in 1 TUBE1 tube2012-12-150000-00-00NoNoCurrent
0065-0474-02000650474023.5 g in 1 TUBE3.5 gHistorical