ImproVue
- Product NDC
- 62144-5510
- 11-digit product format
- 621445510
- Labeler code
- 62144
- Product ID
- 62144-5510_8d8a7585-2067-470f-912c-e62ab6277ec2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- HYPROMELLOSE 2208 (15000 MPA.S)
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Oculus Surgical, Inc.
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-06-25
- Substance
- HYPROMELLOSE 2208 (15000 MPA.S)
- Active strength
- 17 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ImproVue
- Brand name suffix
- Lubricant
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYPROMELLOSE 2208 (15000 MPA.S) | 17 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Z78RG6M2N2 |
| Rxcui | 1540361 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62144-5510-5 | ImproVueLubricant | 6 in 1 CARTON | SOLUTION/ DROPS | 6 | | 5 |
| 62144-5510-5 | ImproVueLubricant | 1 in 1 POUCH | SOLUTION/ DROPS | 1 | | 5 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| HYPROMELLOSE 2208 (15000 MPA.S) | ACTIVE INGREDIENT | Z78RG6M2N2 | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| HYPROMELLOSE 2208 (15000 MPA.S) | ACTIVE MOIETY | Z78RG6M2N2 | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| Calcium Chloride | INACTIVE INGREDIENT | M4I0D6VV5M | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| Hydrochloric Acid | INACTIVE INGREDIENT | QTT17582CB | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| Magnesium Chloride | INACTIVE INGREDIENT | 02F3473H9O | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| Potassium Chloride | INACTIVE INGREDIENT | 660YQ98I10 | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| Sodium Acetate | INACTIVE INGREDIENT | 4550K0SC9B | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| Sodium Chloride | INACTIVE INGREDIENT | 451W47IQ8X | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| Sodium Hydroxide | INACTIVE INGREDIENT | 55X04QC32I | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| Trisodium Citrate Dihydrate | INACTIVE INGREDIENT | B22547B95K | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | IMPROVUE (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62144-5510 | IMPROVUE LUBRICANT (HYPROMELLOSE 2208 (15000 MPA.S)) SOLUTION/ DROPS [OCULUS SURGICAL, INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250124_63b82129-4848-47c5-bf92-ec4b1a9e9974.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62144-5510-5 | 62144551005 | 6 POUCH in 1 CARTON (62144-5510-5) / 1 SYRINGE, PLASTIC in 1 POUCH / 2 mL in 1 SYRINGE, PLASTIC | 6 pouch | 2014-06-25 | 0000-00-00 | No | No | Current |