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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.