Home NDC 47682-193 Medi-First Lubricant Eye Drops
Product NDC 47682-193
11-digit product format 476820193
Labeler code 47682
Product ID 47682-193_4735597f-6299-c349-e063-6294a90a09ec
Type HUMAN OTC DRUG
Nonproprietary name Carboxymethylcellulose sodium
Dosage form SOLUTION
Route OPHTHALMIC
Labeler Unifirst First Aid Corporation
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-01
Substance CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
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 Medi-First Lubricant Eye Drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM .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 47682-193-83 Medi-First Lubricant Eye Drops 30 in 1 BOX SOLUTION 30 7 47682-193-83 Medi-First Lubricant Eye Drops 0.4 mL in 1 AMPULE SOLUTION 0.4 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 47682-193 MEDI-FIRST LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION [UNIFIRST FIRST AID CORPORATION] 5 Current NDC, Legacy NDC, 2 package rows 20250101_a4e651cc-adf0-af9e-e053-2995a90ace5a.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 Units Marketing start Marketing end Sample Exclude flag Status 47682-193-83 47682019383 30 AMPULE in 1 BOX (47682-193-83) / .4 mL in 1 AMPULE 30 ampule 2020-09-01 0000-00-00 No No Current