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 | Type |
|---|---|---|---|
| Leader Dry Eye Relief Eye Drops (PLD) | CARDINAL HEALTH 110, LLC. DBA LEADER | KC Pharmaceuticals, Inc. | 2026-08-17 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70000-0502-1 | Leader Dry Eye Relief Eye Drops | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | 7 | |
| 70000-0502-1 | Leader Dry Eye Relief Eye Drops | 15 mL in 1 BOTTLE, PLASTIC | SOLUTION/ DROPS | 15 | 7 | |
| 70000-0502-2 | Leader Dry Eye Relief Eye Drops | 2 in 1 CARTON | SOLUTION/ DROPS | 2 | 7 | |
| 70000-0502-2 | Leader Dry Eye Relief Eye Drops | 15 mL in 1 BOTTLE, PLASTIC | SOLUTION/ DROPS | 15 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70000-0502 | LEADER DRY EYE RELIEF EYE DROPS (GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400) SOLUTION/ DROPS [CARDINAL HEALTH] | 5 | Current NDC, Legacy NDC, 4 package rows | 20240104_2ded4bda-b3c3-4521-8701-5c8446fd148b.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70000-0502-1 | ML - Milliliter | 70000-0502 | 1f203b31-da5d-4e94-9c33-96546f6e91ec | 1 | 2020-02-13 |
| 70000-0502-2 | ML - Milliliter | 70000-0502 | cf12542e-c79c-433c-bb69-279435fa1c48 | 1 | 2020-04-20 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| CVS Maximum OTC Strength Hemorrhoidal with Aloe | GLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, WHITE PETROLATUM | CVS PHARMACY,INC | b55c63fb-5dfa-4567-8192-58f403868837 | 2026-01-02 | Warnings | PDC6A3C0OX |
| Wipex Sanitizing Wipes | BENZALKONIUM CHLORIDE | Unico | 476d7085-82d8-5e84-e063-6394a90a6448 | 2026-01-02 | Warnings | F5UM2KM3W7 |
| Max OUT | BENZALKONIUM CHLORIDE | Unico | 475903d2-a0b0-5d29-e063-6394a90a528f | 2026-01-01 | Warnings | F5UM2KM3W7 |
| VISTA Hypromellose Dry Eye Relief | HYPROMELLOSE | Red Wedding LLC | b2c4954c-ed53-778a-e053-2a95a90ae0d0 | 2026-01-01 | Warnings | M018 |
| Antiseptic wipe | BENZALKONIUM CHLORIDE | Yiwu Ori-Power Medtech Co.,Ltd. | fc4fc127-3130-4891-b390-6dc823cb30d4 | 2026-01-01 | Warnings | F5UM2KM3W7 |
| Potassium Chloride | POTASSIUM CHLORIDE | Northwind Health Company, LLC | f2b671c9-9874-2668-e053-2a95a90a1b46 | 2026-01-01 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride | POTASSIUM CHLORIDE | Northwind Health Company, LLC | f3081031-8234-5732-e053-2995a90aebeb | 2026-01-01 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride | POTASSIUM CHLORIDE | Northwind Health Company, LLC | dae7c63d-eef0-58d0-e053-2a95a90a667e | 2026-01-01 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride | POTASSIUM CHLORIDE | Northwind Health Company, LLC | db4dc4ab-e0d4-7dc7-e053-2995a90ac46e | 2026-01-01 | Warnings, Adverse reactions | 660YQ98I10 |
| Eye Clean | EYE WASH | HART Health | 41f53e2e-c2bc-4bf1-a541-3bcb2cf63002 | 2025-12-31 | Warnings | 059QF0KO0R |
| Ecolab Foaming Hand Sanitizer | BENZALKONIUM CHLORIDE | Ecolab Inc. | 7bc85519-64cb-48a3-bbd6-73e03b1d0611 | 2025-12-31 | Warnings | F5UM2KM3W7 |
| BZK Antiseptic Towelette | BENZALKONIUM CHLORIDE CLOTH | JINHUA JINGDI MEDICAL SUPPLIES CO., LTD | 470fca9f-a819-2290-e063-6294a90abad8 | 2025-12-31 | Warnings | F5UM2KM3W7 |
| Colirio Ojo De Aguila Eye Drops | GLYCERIN, NAPHAZOLINE HYDROCHLORIDE | Grandall Distributing Co., Inc. | 31aa07e9-0cc9-2a77-e063-6394a90a4b9d | 2025-12-31 | Warnings | M018 PDC6A3C0OX |
| B03 Sinus Relief | ALLIUM CEPA, CALCAREA IODATA, CALCAREA SULPHURICA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, EUPHORBIUM OFFICINARUM, HEPAR SULPHURIS CALCAREUM, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, KALI MURIATICUM, KALI SULPHURICUM, LAC DEFLORATUM, LUFFA OPERCULATA, MERCURIUS SULPHURATUS RUBER, PHOSPHORUS, PULSATILLA VULGARIS, SACCHARUM LACTIS, THUJA OCCIDENTALIS | Apex Energetics Inc. | bad83f77-e9ae-7118-e053-2a95a90aa737 | 2025-12-31 | Warnings | 660YQ98I10 |
| Biopure Anti-bacterial Hand Wipes Fresh Morning Breeze Scent | BENZALKONIUM CHLORIDE | Quest USA Corp | f6130f88-a274-4068-9d8e-5f898b3b074f | 2025-12-31 | Warnings | F5UM2KM3W7 |
| Biopure Anti-bacterial Hand Wipes Honey Wildflower Scent | BENZALKONIUM CHLORIDE | Quest USA Corp | d5db76a3-871e-4110-afc3-80f84a77eb2b | 2025-12-31 | Warnings | F5UM2KM3W7 |
| BioPure Antibacterial Hand Wipes Benzalkonium Chloride 0.12% - 250 Wipes | BENZALKONIUM CHLORIDE | QUEST USA CORP. | ae2fdb32-05c6-6d16-e053-2995a90a552d | 2025-12-31 | Warnings | F5UM2KM3W7 |
| Antibacterial Lidocaine Wound Gel | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | Water-Jel Technologies, LLC | ef1a6100-7f78-1fdb-e053-2a95a90abf20 | 2025-12-31 | Warnings | F5UM2KM3W7 |
| Immune Boost | CHERRY PLUM, FERR PHOS, HORNBEAM, KALI SULPH, NAT MUR, OAK, OLIVE, THYMUS (CALF), ZINC MUR | Siddha Flower Essences LLC | e8d44b65-47ef-ebc7-e053-2995a90a8583 | 2025-12-31 | Warnings | 451W47IQ8X |
| Biopure Pocket Size Singles Fresh Breeze Scent | BENZALKONIUM CHLORIDE | Quest USA Corp | d618e4fc-a37d-417f-8b4d-90bb31280cff | 2025-12-31 | Warnings | F5UM2KM3W7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.