Home NDC 70000-0018 Leader Eye Wash
Product NDC 70000-0018
11-digit product format 700000018
Labeler code 70000
Product ID 70000-0018_0d37dad1-2198-7c25-e063-6394a90a7eb7
Type HUMAN OTC DRUG
Nonproprietary name purified water
Dosage form SOLUTION
Route OPHTHALMIC
Labeler Cardinal Health
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-09
Substance WATER
Active strength 99.05 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Leader Eye Wash
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength WATER 99.05 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 059QF0KO0R Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1053429 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70000-0018-1 Leader Eye Wash 118 mL in 1 BOTTLE, DROPPER SOLUTION 118 4 70000-0018-1 Leader Eye Wash 1 in 1 BOX SOLUTION 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0018 LEADER EYE WASH (PURIFIED WATER) SOLUTION [CARDINAL HEALTH] 4 Current NDC, Legacy NDC, 2 package rows 20240103_8d3ad11f-1945-f838-e053-2995a90a7aa5.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 25 of 25 · 486 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join REFRESH TEARS CARBOXYMETHYLCELLULOSE SODIUM Allergan, Inc. 329d1fe0-4432-4565-b7b1-65666bd86526 2022-06-30 Warnings Exact identifier application number: M018 REFRESH Optive Mega-3 CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 Allergan, Inc. c5f2b3f2-2071-45bd-a010-67f848bc0233 2022-06-30 Warnings Exact identifier application number: M018 REFRESH P.M. MINERAL OIL, PETROLATUM Allergan, Inc. 24365d64-cd94-41cc-a7e1-033102d98114 2022-06-30 Warnings Exact identifier application number: M018 REFRESH PLUS CARBOXYMETHYLCELLULOSE SODIUM Allergan, Inc. 0f6a4b4b-cde6-4518-84b5-ce997f1154a7 2022-06-28 Warnings Exact identifier application number: M018 CIRCLE K sterile eye drops TETRAHYDROZOLINE HCL Lil' Drug Store Products, Inc. 2c0e106c-16f6-ff4e-e063-6294a90a7dbb 2018-07-30 Warnings Exact identifier application number: M018 Lil Drug Store Sterile Eye Drops Redness Reliever TETRAHYDROZOLINE HCL Lil' Drug Store Products, Inc. 2c0ea35c-ac52-1043-e063-6394a90a061c 2018-04-30 Warnings Exact identifier application number: M018
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 70000-0018-1 70000001801 1 BOTTLE, DROPPER in 1 BOX (70000-0018-1) / 118 mL in 1 BOTTLE, DROPPER 2019-07-09 0000-00-00 No No Current