NDC 70000-0502-01 - Leader Dry Eye Relief Eye Drops

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
70000-0502
Requested NDC
70000-0502-01
Package NDCs from labels
70000-0502-1, 70000-0502-2, 70000-0502-01
Manufacturer
CARDINAL HEALTH 110, LLC. DBA LEADER | KC Pharmaceuticals, Inc.
Effective date
2026-08-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Leader Dry Eye Relief Eye Drops (PLD)CARDINAL HEALTH 110, LLC. DBA LEADER | KC Pharmaceuticals, Inc.2026-08-17HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70000-0502-1Leader Dry Eye Relief Eye Drops1 in 1 CARTONSOLUTION/ DROPS17
70000-0502-1Leader Dry Eye Relief Eye Drops15 mL in 1 BOTTLE, PLASTICSOLUTION/ DROPS157
70000-0502-2Leader Dry Eye Relief Eye Drops2 in 1 CARTONSOLUTION/ DROPS27
70000-0502-2Leader Dry Eye Relief Eye Drops15 mL in 1 BOTTLE, PLASTICSOLUTION/ DROPS157

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70000-0502LEADER DRY EYE RELIEF EYE DROPS (GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400) SOLUTION/ DROPS [CARDINAL HEALTH]5Current NDC, Legacy NDC, 4 package rows20240104_2ded4bda-b3c3-4521-8701-5c8446fd148b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70000-0502-1ML - Milliliter70000-05021f203b31-da5d-4e94-9c33-96546f6e91ec12020-02-13
70000-0502-2ML - Milliliter70000-0502cf12542e-c79c-433c-bb69-279435fa1c4812020-04-20

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 46 of 165 · 3,300 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DE LA CRUZ SODIUM BICARBONATE ANTACIDSODIUM BICARBONATEDLC Laboratories, Inc.fc469943-9749-45ee-93f7-90fdbcdc72152026-01-07WarningsExact identifier
unii: 8MDF5V39QO
De La Cruz DesempachoSODIUM BICARBONATEDLC LABORATORIES, INC.741e105a-3ed2-4fc7-ab06-273e515a2d162026-01-07WarningsExact identifier
unii: 8MDF5V39QO
Biopure Antibacterial Hand Wipe Juicy WatermelonBENZALKONIUM CHLORIDEQuest USA Corp47d53645-4ba8-0cdc-e063-6294a90a38922026-01-07WarningsExact identifier
unii: F5UM2KM3W7
Biopure Antibacterial Hand Wipe Berry StrawberryBENZALKONIUM CHLORIDEQuest USA Corp47d6574c-0d4c-392e-e063-6394a90a590f2026-01-07WarningsExact identifier
unii: F5UM2KM3W7
Biopure Antibacterial Hand Wipe Vallina DreamBENZALKONIUM CHLORIDEQuest USA Corp47d7090d-036b-870b-e063-6394a90a80c32026-01-07WarningsExact identifier
unii: F5UM2KM3W7
Sodium chlorideSODIUM CHLORIDEBECTON DICKINSON AND COMPANYd39b7307-df67-4e68-acb0-2eda5dc612152026-01-07Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
TheraTears Dry and TiredCARBOXYMETHYLCELLULOSE SODIUMMEDTECH PRODUCTS INC02b70e2d-8159-4637-a282-9eac1468e7862026-01-07WarningsExact identifier
application number: M018
Potassium ChloridePOTASSIUM CHLORIDEHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23b10bd6-11bc-495e-bb05-ec332a9b3f212026-01-06Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
99 Plus Hand SanitizerBENZEALKONIUM CHLORIDEMomar Incorporatedf972a8f1-c928-4e4b-a8dd-a2fb77052d212026-01-06WarningsExact identifier
unii: F5UM2KM3W7
QS Plus Plus Instant Hand SanitizerBENZEALKONIUM CHLORIDEABC Compounding Co., Inc.343f9139-47bc-44b0-9da1-d9d6f6334bc72026-01-06WarningsExact identifier
unii: F5UM2KM3W7
Biopure Anti-bacterial Hand Wipes Fresh Morning Breeze ScentBENZALKONIUM CHLORIDEQuest USA Corp47c105a8-7c76-9cde-e063-6294a90a92842026-01-06WarningsExact identifier
unii: F5UM2KM3W7
Proctozone-GGLYCERINRising Pharma Holdings, Inc.8a5c8ad5-3619-4971-967d-165270a20bc82026-01-06WarningsExact identifier
unii: PDC6A3C0OX
Proctozone GMaxGLYCERINRising Pharma Holdings, Inc.a13c2be6-d650-4b53-bddd-d55e92fe10c62026-01-06WarningsExact identifier
unii: PDC6A3C0OX
Good Sense Hemorrhoidal Maximum Strength Pain ReliefGLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUML. Perrigo Company1d6142b6-3746-46f1-99ec-4b19d26f056e2026-01-06WarningsExact identifier
unii: PDC6A3C0OX
Potassium Chloride for Oral SolutionPOTASSIUM CHLORIDE FOR ORAL SOLUTIONBPI Labs LLC1ea4345e-f8bb-4d41-9003-c87b21169d7c2026-01-05Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Antiseptic Cleaning wipeANTISEPTIC CLEANING WIPESHENZHEN BENLIJU BIO-TECH CO.,LTD203d01ae-d99e-bce3-e063-6294a90a1a2d2026-01-05WarningsExact identifier
unii: F5UM2KM3W7
Sting Relief prep PadSTING RELIEF PREP PADSHENZHEN BENLIJU BIO-TECH CO.,LTD202c7b77-1a48-52a5-e063-6394a90a2eb22026-01-05WarningsExact identifier
unii: PDC6A3C0OX
Skin Cleaning Care WipesSKIN CLEANING CARE WIPESSHENZHEN BENLIJU BIO-TECH CO.,LTD203d7a95-65fe-ca65-e063-6294a90acc6e2026-01-05WarningsExact identifier
unii: PDC6A3C0OX
Hand wipesHAND WIPESSHENZHEN BENLIJU BIO-TECH CO.,LTD39f3acca-7275-88ca-e063-6394a90ad1a22026-01-05WarningsExact identifier
unii: F5UM2KM3W7
Lung DrainageANTIMONIUM ARSENICICUM, BRYONIA (ALBA), CAMPHORA, CARBO VEGETABILIS, CHELIDONIUM MAJUS, CHININUM MURIATICUM, CUPRUM METALLICUM, GELSEMIUM SEMPERVIRENS, HAEMOPHILUS INFLUENZAE B, IPECACUANHA, KALI MURIATICUM, LOBELIA PURPURESCENS, LUNG (SUIS), MYCOPLASMA PNEUMONIAE, MYCOPLASMA PNEUMONIAE DNA, OXYGENIUM, PHOSPHORUS, PNEUMOCOCCINUM, SENEGA OFFICINALIS, STANNUM METALLICUM, VERATRUM VIRIDEDeseret Biologicals, Inc.64a99cd3-341a-44ec-b4eb-c06982e6d4142026-01-05WarningsExact identifier
unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.