iVIZIA Lubricant Eye Gel
- Product NDC
- 82584-701
- 11-digit product format
- 825840701
- Labeler code
- 82584
- Product ID
- 82584-701_509e6e7c-bb53-f135-e063-6294a90a5279
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- povidone
- Dosage form
- GEL
- Route
- OPHTHALMIC
- Labeler
- Thea Pharma Inc.
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-01
- Substance
- POVIDONE, UNSPECIFIED
- Active strength
- 2.5 mg/.5g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
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
- iVIZIA Lubricant Eye Gel
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| POVIDONE, UNSPECIFIED | 2.5 mg/.5g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| FZ989GH94E | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1f06ca1a-5270-9a82-e063-6294a90aed64 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6084a4f4-5437-c9a5-caec-5361ee075a59 | Product name | 1 | 20140508 |
| 90c5639a-61b0-88d6-ddcf-21888e94869a | Product name | 1 | 20140508 |
| 9514609b-a2a9-f8ec-6ba6-3f8e5ee89877 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82584-701-12 | iVIZIA Lubricant Eye Gel | 30 in 1 CARTON | GEL | 30 | 3 | |
| 82584-701-12 | iVIZIA Lubricant Eye Gel | 0.4 g in 1 VIAL, SINGLE-USE | GEL | 0.4 | 3 | |
| 82584-701-60 | iVIZIA Lubricant Eye Gel | 0.4 g in 1 VIAL, SINGLE-USE | GEL | 0.4 | 3 | |
| 82584-701-60 | iVIZIA Lubricant Eye Gel | 30 in 1 CARTON | GEL | 30 | 3 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| REFRESH TEARS | CARBOXYMETHYLCELLULOSE SODIUM | Allergan, Inc. | 329d1fe0-4432-4565-b7b1-65666bd86526 | 2022-06-30 | Warnings | M018 |
| REFRESH Optive Mega-3 | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 | Allergan, Inc. | c5f2b3f2-2071-45bd-a010-67f848bc0233 | 2022-06-30 | Warnings | M018 |
| REFRESH P.M. | MINERAL OIL, PETROLATUM | Allergan, Inc. | 24365d64-cd94-41cc-a7e1-033102d98114 | 2022-06-30 | Warnings | M018 |
| REFRESH PLUS | CARBOXYMETHYLCELLULOSE SODIUM | Allergan, Inc. | 0f6a4b4b-cde6-4518-84b5-ce997f1154a7 | 2022-06-28 | Warnings | M018 |
| CIRCLE K sterile eye drops | TETRAHYDROZOLINE HCL | Lil' Drug Store Products, Inc. | 2c0e106c-16f6-ff4e-e063-6294a90a7dbb | 2018-07-30 | Warnings | M018 |
| Lil Drug Store Sterile Eye Drops Redness Reliever | TETRAHYDROZOLINE HCL | Lil' Drug Store Products, Inc. | 2c0ea35c-ac52-1043-e063-6394a90a061c | 2018-04-30 | Warnings | M018 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 2623248 | iVizia 0.5 % Ophthalmic Gel | PSN | 1f06ca1a-5270-9a82-e063-6294a90aed64 | 3 |
| 2623245 | povidone 0.5 % Ophthalmic Gel | PSN | 1f06ca1a-5270-9a82-e063-6294a90aed64 | 3 |
| 2623248 | povidone 0.005 MG/MG Ophthalmic Gel [iVizia] | SBD | 1f06ca1a-5270-9a82-e063-6294a90aed64 | 3 |
| 2623245 | povidone 0.005 MG/MG Ophthalmic Gel | SCD | 1f06ca1a-5270-9a82-e063-6294a90aed64 | 3 |
| 2623248 | iVizia 0.005 MG/MG Ophthalmic Gel | SY | 1f06ca1a-5270-9a82-e063-6294a90aed64 | 3 |
| 2623248 | iVizia 0.5 % Ophthalmic Gel | SY | 1f06ca1a-5270-9a82-e063-6294a90aed64 | 3 |
| 2623245 | povidone 0.5 % Ophthalmic Gel | SY | 1f06ca1a-5270-9a82-e063-6294a90aed64 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 82584-701-12 | 82584070112 | 30 VIAL, SINGLE-USE in 1 CARTON (82584-701-12) / .4 g in 1 VIAL, SINGLE-USE | 2024-12-01 | No | No | Current |
| 82584-701-60 | 82584070160 | 30 VIAL, SINGLE-USE in 1 CARTON (82584-701-60) / .4 g in 1 VIAL, SINGLE-USE | 2026-04-30 | Yes | No | Current |