Home NDC 70000-0090 Lubricant Drops
Product NDC 70000-0090
11-digit product format 700000090
Labeler code 70000
Product ID 70000-0090_7032f298-3bfe-4fd2-b240-36ec6015ffbe
Type HUMAN OTC DRUG
Nonproprietary name carboxymethylcellulose sodium
Dosage form SOLUTION/ DROPS
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 5 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 Lubricant Drops CARBOXYMETHYLCELLULOSE SODIUM CARDINAL HEALTH 110, LLC. DBA LEADER 1ac2fe24-9ff6-48c1-b123-fbc0e48f5304 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 Lubricant Drops Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 5 mg/mL
Harmonized Identifiers# Field, Values table Field Values Unii K679OBS311 Rxcui 1188426
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 70000-0090-1 Lubricant Drops 1 in 1 CARTON SOLUTION/ DROPS 1 4 70000-0090-1 Lubricant Drops 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 4 70000-0090-2 Lubricant Drops 2 in 1 CARTON SOLUTION/ DROPS 2 4 70000-0090-2 Lubricant Drops 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0090 LUBRICANT DROPS (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [CARDINAL HEALTH, 110 DBA LEADER] 3 Current NDC, Legacy NDC, 4 package rows 20210701_1ac2fe24-9ff6-48c1-b123-fbc0e48f5304.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 70000-0090-1 70000009001 1 BOTTLE, DROPPER in 1 CARTON (70000-0090-1) / 15 mL in 1 BOTTLE, DROPPER 2021-03-09 2026-11-30 No No Current 70000-0090-2 70000009002 2 BOTTLE, DROPPER in 1 CARTON (70000-0090-2) / 15 mL in 1 BOTTLE, DROPPER 2021-03-09 2026-11-30 No No Current