Lubricant Eye Drops Preservative free 30 Single Use Container

Product NDC
73450-002
11-digit product format
734500002
Labeler code
73450
Product ID
73450-002_9f57f9b5-e975-0365-e053-2a95a90adbbd
Type
HUMAN OTC DRUG
Nonproprietary name
CARBOXYMETHYLCELLULOSE SODIUM
Dosage form
LIQUID
Route
OPHTHALMIC
Labeler
Nexus Optical Inc
Application
part349
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2020-04-20
Marketing end
0000-00-00
Substance
CARBOXYMETHYLCELLULOSE SODIUM
Active strength
5 mg/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

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
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct 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
73450-002-052022-01-28C16284748780-1d6a99b39-bbe9-a426-e053-dadaa90af4c2Lubricant Eye Drops Preservative-free, 30 Single Use Container

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73450-002-05Lubricant Eye Drops Preservative free 30 Single Use Container30 in 1 BOXLIQUID301
73450-002-05Lubricant Eye Drops Preservative free 30 Single Use Container0.5 mL in 1 VIAL, SINGLE-USELIQUID0.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73450-002LUBRICANT EYE DROPS PRESERVATIVE FREE 30 SINGLE USE CONTAINER (CARBOXYMETHYLCELLULOSE SODIUM) LIQUID [NEXUS OPTICAL INC]1Legacy NDC, 2 package rows20200420_9f57f9b5-e974-0365-e053-2a95a90adbbd.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionPSN9f57f9b5-e974-0365-e053-2a95a90adbbd1
1188426carboxymethylcellulose sodium 5 MG/ML Ophthalmic SolutionSCD9f57f9b5-e974-0365-e053-2a95a90adbbd1
1188426carboxymethylcellulose sodium 0.5 % Ophthalmic SolutionSY9f57f9b5-e974-0365-e053-2a95a90adbbd1
1188426carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic SolutionSY9f57f9b5-e974-0365-e053-2a95a90adbbd1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
73450-002-057345000020530 VIAL, SINGLE-USE in 1 BOX (73450-002-05) > .5 mL in 1 VIAL, SINGLE-USE2020-04-200000-00-00NoNoCurrent