iVizia Dry Eye

Product NDC: 59262-700
Requested package NDC: 59262-700-11
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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	59262-700	59262-700-11	D	Discontinued by firm		2026-10-15

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 · 6 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`

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 concept	Relation	Version	Effective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75	Product name	2	20250814

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Indexing SPL table
NDC	Effective	Indexing SPL	Related label
59262-700-05	2023-08-10	f386c64a-2682-0266-e053-dadaa90a7c1a	iVizia Dry Eye Drops
59262-700-11	2023-08-09	f386c649-a8bd-0266-e053-dadaa90a7c1a	iVizia Dry Eye Drops 10ml
59262-700-05	2023-01-30	f386c64a-2682-0266-e053-dadaa90a7c1a	iVizia Dry Eye Drops
59262-700-11	2023-01-30	f386c649-a8bd-0266-e053-dadaa90a7c1a	iVizia Dry Eye Drops 10ml

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59262-700	IVIZIA DRY EYE (POVIDONE) SOLUTION/ DROPS [SIMILASAN CORPORATION]	9	Legacy NDC	20241207_e53c6293-24f3-48e4-b5c0-1f1857580649.zip
59262-700	IVIZIA DRY EYE (POVIDONE) SOLUTION/ DROPS [SIMILASAN CORPORATION]	7	Legacy NDC	20241207_7f856543-d724-4548-b91b-b1b6d613caa5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59262-700-11	59262070011	10 mL in 1 BOTTLE, DROPPER (59262-700-11)	10 ml	2021-11-29	0000-00-00	Yes	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
iVizia Dry Eye Drops	Similasan Corporation	2024-12-03	HUMAN OTC DRUG LABEL	9
iVizia Dry Eye Drops 10ml	Similasan Corporation	2024-12-03	HUMAN OTC DRUG LABEL	8
iVizia Dry Eye Drops 5ml Sample	Similasan Corporation	2024-12-03	HUMAN OTC DRUG LABEL	7