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 25 of 25 · 486 matching rows.
Brand, Generic, Manufacturer table 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 Exact identifier application number: M018 REFRESH Optive Mega-3 CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 Allergan, Inc. c5f2b3f2-2071-45bd-a010-67f848bc0233 2022-06-30 Warnings Exact identifier application number: M018 REFRESH P.M. MINERAL OIL, PETROLATUM Allergan, Inc. 24365d64-cd94-41cc-a7e1-033102d98114 2022-06-30 Warnings Exact identifier application number: M018 REFRESH PLUS CARBOXYMETHYLCELLULOSE SODIUM Allergan, Inc. 0f6a4b4b-cde6-4518-84b5-ce997f1154a7 2022-06-28 Warnings Exact identifier application number: M018 CIRCLE K sterile eye drops TETRAHYDROZOLINE HCL Lil' Drug Store Products, Inc. 2c0e106c-16f6-ff4e-e063-6294a90a7dbb 2018-07-30 Warnings Exact identifier application number: 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 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