Home NDC 56062-666-01 Publix Artificial Tears Eye Drops
Product NDC 56062-666
Requested package NDC 56062-666-01
11-digit product format 560620666
Labeler code 56062
Product ID 56062-666_4748e087-e0d9-aa44-e063-6294a90a675a
Type HUMAN OTC DRUG
Nonproprietary name polyvinyl alcohol, povidone
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Publix Super Markets, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-03-20
Substance POLYVINYL ALCOHOL; POVIDONE
Active strength 500; 600 mg/100mL; mg/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 Publix Artificial Tears Eye Drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POLYVINYL ALCOHOL 500 mg/100mL POVIDONE 600 mg/100mL
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 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 56062-666-01 Publix Artificial Tears Eye Drops 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 3 56062-666-01 Publix Artificial Tears 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 56062-666 PUBLIX ARTIFICIAL TEARS EYE DROPS (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [PUBLIX SUPER MARKETS, INC.] 2 Current NDC, 2 package rows 20231224_f5d1394b-0fe8-c372-e053-2a95a90a1f78.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 Sample Exclude flag Status 56062-666-01 56062066601 1 BOTTLE, DROPPER in 1 BOX (56062-666-01) / 15 mL in 1 BOTTLE, DROPPER 2023-03-20 No No Current