FDA.reportPublic FDA data

iVizia Dry Eye

Product NDC
59262-700
Requested package NDC
59262-700-05
11-digit product format
592620700
Labeler code
59262
Product ID
59262-700_2436e3c5-f23a-4551-b7d5-776b40437ab4
Type
HUMAN OTC DRUG
Nonproprietary name
Povidone
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
Similasan Corporation
Application
part349
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-11-29
Marketing end
0000-00-00
Substance
POVIDONE
Active strength
50 mg/10mL
NDC exclude flag
No
Listing certified through
2022-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage59262-70059262-700-05DDiscontinued 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 · 1 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage59262-70059262-700-05DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Indexing SPL table
NDCEffectiveIndexing SPLRelated label
59262-700-052023-08-10f386c64a-2682-0266-e053-dadaa90a7c1aiVizia Dry Eye Drops
59262-700-112023-08-09f386c649-a8bd-0266-e053-dadaa90a7c1aiVizia Dry Eye Drops 10ml
59262-700-052023-01-30f386c64a-2682-0266-e053-dadaa90a7c1aiVizia Dry Eye Drops
59262-700-112023-01-30f386c649-a8bd-0266-e053-dadaa90a7c1aiVizia Dry Eye Drops 10ml

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59262-700IVIZIA DRY EYE (POVIDONE) SOLUTION/ DROPS [SIMILASAN CORPORATION]9Legacy NDC20241207_e53c6293-24f3-48e4-b5c0-1f1857580649.zip
59262-700IVIZIA DRY EYE (POVIDONE) SOLUTION/ DROPS [SIMILASAN CORPORATION]7Legacy NDC20241207_7f856543-d724-4548-b91b-b1b6d613caa5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59262-700-05592620700055 mL in 1 BOTTLE, DROPPER (59262-700-05) 5 ml2021-11-290000-00-00NoNoCurrent