Home NDC 41250-819 Meijer Artificial Tears
Product NDC 41250-819
11-digit product format 412500819
Labeler code 41250
Product ID 41250-819_0d22c2c2-a706-2509-e063-6294a90ae206
Type HUMAN OTC DRUG
Nonproprietary name Polyvinyl alcohol, Povidone
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Meijer Distribution, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-04-21
Substance POVIDONE; POLYVINYL ALCOHOL, UNSPECIFIED
Active strength .6; .5 g/100mL; g/100mL
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 Meijer Artificial Tears
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POVIDONE .6 g/100mL POLYVINYL ALCOHOL, UNSPECIFIED .5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination FZ989GH94E Internal UNII lookup 532B59J990 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 598050 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-819-01 Meijer Artificial Tears 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 3 41250-819-01 Meijer Artificial Tears 1 in 1 BOX SOLUTION/ DROPS 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-819 MEIJER ARTIFICIAL TEARS (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [MEIJER DISTRIBUTION, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20231223_9feb3eec-a36f-8fc7-e053-2a95a90adcd3.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 41250-819-01 41250081901 1 BOTTLE, DROPPER in 1 BOX (41250-819-01) / 15 mL in 1 BOTTLE, DROPPER 2020-04-21 0000-00-00 No No Current