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 |
|---|---|---|---|---|---|---|
| Regener-Eyes Ophthalmic Solution PROFESSIONAL | GLYCERIN OPHTHALMIC SOLUTION | M & M PRODUCTS, LLC | 49771efa-6682-51d0-e063-6294a90a18a5 | 2026-01-28 | Warnings | M018 PDC6A3C0OX |
| Regener-Eyes Ophthalmic Solution LITE | GLYCERIN OPHTHALMIC SOLUTION | M & M PRODUCTS, LLC | 497763ee-dc70-bb48-e063-6294a90afb3d | 2026-01-28 | Warnings | M018 PDC6A3C0OX |
| ADRIAN BICARBONATO SODIUM BICARBONATE USP-4 oz, 8 oz and 16 oz | SODIUM BICARBONATE | Evi Labs | 4979a339-4ad4-9cdd-e063-6394a90a0acc | 2026-01-28 | Warnings | 8MDF5V39QO |
| Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Gel/Drops | HYPROMELLOSE OPHTHALMIC SOLUTION 2% W/V | Aurolab | f27a6799-e2f1-ee8d-e053-2a95a90aead1 | 2026-01-27 | Warnings | M018 |
| Carboxymethylcellulose Sodium Eye Drops 0.5% | CARBOXYMETHYLCELLULOSE SODIUM EYE DROPS 0.5% | Aurolab | e8b4df3b-3d81-b3ca-e053-2a95a90af2ec | 2026-01-27 | Warnings | M018 |
| Aurovisc OE | HYPROMELLOSE OPHTHALMIC SOLUTION 2% W/V | Aurolab | 3142c6df-77ac-ec41-e063-6294a90aee47 | 2026-01-27 | Warnings | M018 |
| AURO-CMC | CARBOXYMETHYLCELLULOSE EYE DROPS 0.5% | Aurolab | e90b397f-fe64-8674-e053-2995a90a223f | 2026-01-27 | Warnings | M018 |
| Optase Allegro | HYDROXYETHYL CELLULOSE | Scope Health Inc | f7999928-f5c1-98d6-e053-6294a90a57db | 2026-01-27 | Warnings | M018 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 4906f079-8c9f-e3b0-e063-6294a90ad0f8 | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 4912b681-e21a-1ddf-e063-6294a90aa9f4 | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 491a6d77-8a84-c76d-e063-6394a90ac61f | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 491b55ca-2c7a-0eb7-e063-6394a90a9cb7 | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 491c4af8-c699-7128-e063-6294a90ae0f9 | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 491de8ca-07e7-0aa3-e063-6394a90ae36f | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 492793db-7dc2-8313-e063-6394a90a52bf | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 4928615e-d1a9-72b8-e063-6394a90aa7ed | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 4943e51a-bb8e-745a-e063-6294a90a0a3d | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Anti-bacterial Hand Wipes | ANTI-BACTERIAL HAND WIPES | Jinhua Aidi Daily Chemical Co., Ltd. | 494b09a4-4982-13bf-e063-6394a90a486f | 2026-01-26 | Warnings | F5UM2KM3W7 |
| Sodium Chloride | SODIUM CHLORIDE | Nephron Pharmaceuticals Corporation | a4edf2d5-a9ff-30d4-e053-2995a90a5650 | 2026-01-26 | Warnings, Adverse reactions | 451W47IQ8X |
| BZK Pads | BENZALKONIUM CHLORIDE | Dynarex Corporation | 87288939-cc34-4437-94ab-dcb997d6acd5 | 2026-01-23 | Warnings | F5UM2KM3W7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.