Home NDC 70000-0089 Dry Eye Relief
Product NDC 70000-0089
11-digit product format 700000089
Labeler code 70000
Product ID 70000-0089_b2fd3f1c-69bb-4c0c-9a11-1c135377045c
Type HUMAN OTC DRUG
Nonproprietary name Carboxymethylcellulose sodium
Dosage form GEL
Route OPHTHALMIC
Labeler CARDINAL HEALTH 110, LLC. DBA LEADER
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-03-09
Marketing end 2026-11-30
Substance CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
Active strength 10 mg/mL
NDC exclude flag No
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Dry Eye Relief CARBOXYMETHYLCELLULOSE SODIUM CARDINAL HEALTH 110, LLC. DBA LEADER bd262028-32e9-052d-e053-2a95a90a5303 2025-09-12 Warnings Exact identifier
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings • For external use only. • To avoid contamination, do not touch tip of container to any surface. Replace cap after using. • If solution changes color or becomes cloudy, do not use. Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Additional Listing Data#
Finished product Yes
Brand name base Dry Eye Relief Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 10 mg/mL
Harmonized Identifiers# Field, Values table Field Values Unii K679OBS311 Rxcui 579907
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70000-0089-1 Dry Eye Relief 1 in 1 CARTON GEL 1 3 70000-0089-1 Dry Eye Relief 15 mL in 1 BOTTLE, DROPPER GEL 15 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0089 DRY EYE RELIEF (CARBOXYMETHYLCELLULOSE SODIUM) GEL [CARDINAL HEALTH, 110 DBA LEADER] 2 Current NDC, Legacy NDC, 2 package rows 20210701_bd262028-32e9-052d-e053-2a95a90a5303.zip
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 70000-0089-1 70000008901 1 BOTTLE, DROPPER in 1 CARTON (70000-0089-1) / 15 mL in 1 BOTTLE, DROPPER 2021-03-09 2026-11-30 No No Current