Home NDC 56062-789 Publix Moisturizing Relief Eye Drops
Product NDC 56062-789
11-digit product format 560620789
Labeler code 56062
Product ID 56062-789_4748e9d7-002c-1bc0-e063-6394a90a9730
Type HUMAN OTC DRUG
Nonproprietary name Carboxymethylcellulose sodium
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Publix Super Markets, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance CARBOXYMETHYLCELLULOSE SODIUM
Active strength .5 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 Publix Moisturizing Relief Eye Drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM .5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K679OBS311 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1188426 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 56062-789-01 Publix Moisturizing Relief Eye Drops 30 in 1 BOX SOLUTION/ DROPS 30 3 56062-789-01 Publix Moisturizing Relief Eye Drops 0.4 mL in 1 VIAL, SINGLE-USE SOLUTION/ DROPS 0.4 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 56062-789 PUBLIX MOISTURIZING RELIEF EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [PUBLIX SUPER MARKETS, INC.] 2 Current NDC, Legacy NDC, 2 package rows 20240103_9b391400-c53b-7c7b-e053-2995a90a2731.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 56062-789-01 56062078901 30 VIAL, SINGLE-USE in 1 BOX (56062-789-01) / .4 mL in 1 VIAL, SINGLE-USE 2020-01-01 0000-00-00 No No Current