Home NDC 50090-2358 REFRESH CLASSIC
Product NDC 50090-2358
11-digit product format 500902358
Labeler code 50090
Product ID 50090-2358_2a6ae637-2f65-4a5f-99d3-e3560f67b8f0
Type HUMAN OTC DRUG
Nonproprietary name Polyvinyl Alcohol, Povidone
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler A-S Medication Solutions
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 1985-09-12
Substance POLYVINYL ALCOHOL; POVIDONE
Active strength 14; 6 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 REFRESH CLASSIC
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POLYVINYL ALCOHOL 14 mg/mL POVIDONE 6 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 532B59J990 Internal UNII lookup FZ989GH94E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 359969 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50090-2358-1 REFRESH CLASSIC 30 in 1 CARTON SOLUTION/ DROPS 30 18 50090-2358-1 REFRESH CLASSIC .4 mL in 1 VIAL, SINGLE-USE SOLUTION/ DROPS .4 18
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50090-2358 REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [A-S MEDICATION SOLUTIONS] 18 Current NDC, Legacy NDC, 2 package rows 20240316_3bf6193c-56db-45ad-844c-58eb8c33cba9.zip
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.
Matched openFDA labels page 17 of 25 · 486 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join OASIS Tears Lubricant Eye GLYCERIN OASIS Medical, Inc. 00071697-4ac6-4962-8eee-388b8b52bd40 2025-01-22 Warnings Exact identifier application number: M018 ImproVue Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Oculus Surgical, Inc. 63b82129-4848-47c5-bf92-ec4b1a9e9974 2025-01-22 Warnings Exact identifier application number: M018 VISCO SHIELD Lubricant HYPROMELLOSE 2208 (15000 MPA.S) OASIS Medical, Inc. 72d22610-d8ab-4f24-b304-8b013430a7d7 2025-01-22 Warnings Exact identifier application number: M018 OASIS Tears Plus Preservative-Free Lubricant Eye GLYCERIN OASIS Medical, Inc. ea931c0f-c61e-4771-84f1-0274b1c3e28e 2025-01-22 Warnings Exact identifier application number: M018 Medics Choice Soothing Eye Wash PURIFIED WATER KC Pharmaceuticals, Inc. 10e49808-161e-f4ec-e063-6294a90a1775 2025-01-19 Warnings Exact identifier application number: M018 Sodium Chloride Hypertonicity Ophthalmic Solution, 5% SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5% Reliable 1 Laboritories LLC 29175c17-223e-5e92-e063-6294a90a71d2 2025-01-15 Warnings Exact identifier application number: M018 Lubricating Tears CARBOXYMETHYLCELLULOSE SODIUM 0.5% SOLUTION Reliable 1 Laboritories LLC 29023a57-eba3-4241-e063-6294a90a7048 2025-01-15 Warnings Exact identifier application number: M018 Aurodone Povidone Iodine 5 % Opthalmic Solution POVIDONE IODINE 5 % TOPICAL SOLUTION Aurolab f3444446-1dad-79ff-e053-2a95a90af411 2025-01-06 Warnings Exact identifier application number: M018 Hypromellose Eye Drops 0.7% HYPROMELLOSE EYE DROPS 0.7% Aurolab d35313d0-b190-5fb0-e053-2a95a90a5283 2025-01-02 Warnings Exact identifier application number: M018 VISTA MEIBO TEARS Propylene Glycol 0.6% w/v Advanced Dry Eye Relief Lubricating Drops 10 ml PROPYLENE GLYCOL Red Wedding LLC b2c2fd0f-b944-6b0b-e053-2995a90aa216 2025-01-01 Warnings Exact identifier application number: M018 Rite Aid Hydration Lubricant Eye Drops POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL Rite Aid Corporation ecac1351-e944-21da-e053-2995a90a6d34 2024-12-31 Warnings Exact identifier application number: M018 Lubricant Eye PM MINERAL OIL, WHITE PETROLATUM Reliable 1 Laboratories LLC baec8045-97fe-6f60-e053-2a95a90a050e 2024-12-31 Warnings Exact identifier application number: M018 Lil Drug Store Eye Drops Redness Reliever TETRAHYDROZOLINE HYDROCHLORIDE Lil Drug Store Products, Inc d2a47e98-a04c-47ec-aded-d1c894f040e2 2024-12-30 Warnings Exact identifier application number: M018 Rain Renewal Eye Drops CARBOXYMETHYLCELLULOSE SODIUM Rain Eye Drops, LLC af7a5768-7d1d-3d93-e053-2a95a90a38f6 2024-12-29 Warnings Exact identifier application number: M018 Glitch Advanced Relief Eye Drops POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL Misemer Pharmaceutical, Inc 03778509-3374-2168-e063-6294a90a9505 2024-12-23 Warnings Exact identifier application number: M018 OASIS Tears Preservative-Free Lubricant Eye GLYCERIN OASIS Medical, Inc. d9d71b1d-82a6-42e7-9ef2-2d041daef936 2024-12-23 Warnings Exact identifier application number: M018 Ancient Secrets Breathe Again SODIUM CHLORIDE LOTUS BRANDS, INC. c6d2bab0-d363-4c09-a71b-ae15db915b37 2024-12-18 Warnings Exact identifier application number: M018 Fendall Pure Flow PURIFIED WATER Honeywell Safety Products USA, Inc. afda6fc3-7615-b0be-e053-2995a90a6208 2024-12-10 Warnings Exact identifier application number: M018 Systane Nighttime MINERAL OIL AND WHITE PETROLATUM Alcon Laboratories, Inc. 4689c59c-5721-3f91-6c85-e41501998fd0 2024-12-05 Warnings Exact identifier application number: M018 GenTeal Tears NIGHT-TIME MINERAL OIL, WHITE PETROLATUM Alcon Laboratories, Inc. 9d5998a7-4f59-4293-87da-8419650a524d 2024-12-05 Warnings Exact identifier application number: M018
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 50090-2358-1 50090235801 30 VIAL, SINGLE-USE in 1 CARTON (50090-2358-1) / .4 mL in 1 VIAL, SINGLE-USE 2016-04-21 0000-00-00 No No Current