Lubricant Eye Plus

Product NDC
11822-0323
11-digit product format
118220323
Labeler code
11822
Product ID
11822-0323_0747eaeb-3e68-4ad0-bfa2-2b978792d569
Type
HUMAN OTC DRUG
Nonproprietary name
carboxymethylcellulose sodium
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Rite Aid Corporation
Application
part349
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2013-09-16
Marketing end
0000-00-00
Substance
CARBOXYMETHYLCELLULOSE SODIUM
Active strength
1 g/100mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct11822-0323DDiscontinued by firm2026-08-10
excluded packagepackage11822-032311822-0323-1DDiscontinued by firm2026-08-10

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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage11822-0323-1d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage11822-0323-1f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage11822-0323-12ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage11822-0323-1a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage11822-0323-1cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage11822-0323-1cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage11822-0323-1302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage11822-0323-1ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage11822-0323-10efc9e666f02…f202fb6c5f17…

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CARBOXYMETHYLCELLULOSE SODIUMACTIVE INGREDIENTK679OBS311LUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1
CARBOXYMETHYLCELLULOSEACTIVE MOIETY05JZI7B19XLUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1
CALCIUM CHLORIDEINACTIVE INGREDIENTM4I0D6VV5MLUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1
HYDROCHLORIC ACIDINACTIVE INGREDIENTQTT17582CBLUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1
MAGNESIUM CHLORIDEINACTIVE INGREDIENT02F3473H9OLUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1
POTASSIUM CHLORIDEINACTIVE INGREDIENT660YQ98I10LUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XLUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32ILUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1
SODIUM LACTATEINACTIVE INGREDIENTTU7HW0W0QTLUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1
WATERINACTIVE INGREDIENT059QF0KO0RLUBRICANT EYE PLUS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION, GEL FORMING / DROPS [RITE AID CORPORATION]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0323-1118220323016 POUCH in 1 CARTON (11822-0323-1) > 5 VIAL, SINGLE-USE in 1 POUCH > .4 mL in 1 VIAL, SINGLE-USE6 pouch2013-09-160000-00-00NoNoCurrent