Home NDC 0023-0506 REFRESH Classic
Product NDC 0023-0506
11-digit product format 000230506
Labeler code 0023
Product ID 0023-0506_58d49977-1915-4473-801d-a28b87b9a328
Type HUMAN OTC DRUG
Nonproprietary name Polyvinyl Alcohol, Povidone
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Allergan, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 1985-09-12
Substance POLYVINYL ALCOHOL, UNSPECIFIED; POVIDONE
Active strength 14; 6 mg/mL; mg/mL
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 REFRESH Classic
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POLYVINYL ALCOHOL, UNSPECIFIED 14 mg/mL POVIDONE 6 mg/mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0023-0506-01 REFRESH Classic 0.4 mL in 1 VIAL, SINGLE-USE SOLUTION/ DROPS 0.4 11 0023-0506-01 REFRESH Classic 30 in 1 CARTON SOLUTION/ DROPS 30 11 0023-0506-50 REFRESH Classic 50 in 1 CARTON SOLUTION/ DROPS 50 11 0023-0506-50 REFRESH Classic 0.4 mL in 1 VIAL, SINGLE-USE SOLUTION/ DROPS 0.4 11
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Polyvinyl Alcohol ACTIVE INGREDIENT 532B59J990 REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.] 4 Povidone ACTIVE INGREDIENT FZ989GH94E REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.] 4 Polyvinyl Alcohol ACTIVE MOIETY 532B59J990 REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.] 4 Povidone ACTIVE MOIETY FZ989GH94E REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.] 4 hydrochloric acid INACTIVE INGREDIENT QTT17582CB REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.] 4 sodium chloride INACTIVE INGREDIENT 451W47IQ8X REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.] 4 sodium hydroxide INACTIVE INGREDIENT 55X04QC32I REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.] 4 water INACTIVE INGREDIENT 059QF0KO0R REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0023-0506 REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.] 10 Current NDC, Legacy NDC, 4 package rows 20240214_31bf1d6c-9719-4060-b6a3-409a2fe7b560.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 6 of 25 · 494 matching rows.
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 0023-0506-01 00023050601 30 VIAL, SINGLE-USE in 1 CARTON (0023-0506-01) / .4 mL in 1 VIAL, SINGLE-USE 1985-09-12 0000-00-00 No No Current 0023-0506-50 00023050650 50 VIAL, SINGLE-USE in 1 CARTON (0023-0506-50) / .4 mL in 1 VIAL, SINGLE-USE 1985-09-12 0000-00-00 No No Current