Home NDC 41250-319 Meijer Lubricant Eye Drops
Product NDC 41250-319
11-digit product format 412500319
Labeler code 41250
Product ID 41250-319_0d2273c9-17e1-0f0b-e063-6294a90a76da
Type HUMAN OTC DRUG
Nonproprietary name Polyethylene glycol 400, Propylene glycol
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Meijer Distribution, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-04-20
Substance PROPYLENE GLYCOL; POLYETHYLENE GLYCOL 400
Active strength .3; .4 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 Lubricant Eye Drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PROPYLENE GLYCOL .3 g/100mL POLYETHYLENE GLYCOL 400 .4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 6DC9Q167V3 Internal UNII lookup B697894SGQ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 477589 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 41250-319-01 Meijer Lubricant Eye Drops 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 3 41250-319-01 Meijer Lubricant Eye Drops 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 41250-319 MEIJER LUBRICANT EYE DROPS (POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL) SOLUTION/ DROPS [MEIJER DISTRIBUTION, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20231223_9feadde4-fbe5-0c9e-e053-2995a90a9b30.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 41250-319-01 41250031901 1 BOTTLE, DROPPER in 1 BOX (41250-319-01) / 15 mL in 1 BOTTLE, DROPPER 2020-04-20 0000-00-00 No No Current