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 |
|---|---|---|---|---|---|---|
| Chemcor Chemical Foaming Hand Sanitizer | BENZALKONIUM CHLORIDE | Chemcor Chemical Corporation | 5c9d90c1-0381-4237-9529-398fa51b3ab4 | 2025-12-22 | Warnings | F5UM2KM3W7 |
| Fresh Hands | BENZALKONIUM CHLORIDE | Maintex | e174083a-8820-4fa7-8cc2-0a2c86f27cd6 | 2025-12-22 | Warnings | F5UM2KM3W7 |
| Redness and Dry Eye Relief | GLYCERIN, NAPHAZOLINE HYDROCHLORIDE | KC Pharmaceuticals, Inc | 4682f68d-6bdd-d860-e063-6394a90a2b52 | 2025-12-21 | Warnings | M018 PDC6A3C0OX |
| Original Redness Reliever | TETRAHYDROLIZINE HCL | KC Pharmaceuticals | 4683b850-b0fc-5093-e063-6294a90aef44 | 2025-12-21 | Warnings | M018 |
| Equate Nighttime Relief Lubricant | LIGHT MINERAL OIL, WHITE PETROLATUM | Walmart | 4449a55b-2cd4-0cb9-e063-6294a90aafbc | 2025-12-20 | Warnings | M018 |
| Equate Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | Walmart | 44494842-e38d-617c-e063-6294a90afaf8 | 2025-12-20 | Warnings | M018 |
| Equate Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN | Walmart | 443e214b-2680-79a9-e063-6294a90a68ba | 2025-12-20 | Warnings | M018 PDC6A3C0OX |
| Equate Redness and Dry Eye Relief | GLYCERIN, NAPHAZOLINE HYDROCHLORIDE | Walmart | 44155cf8-6fd9-d16f-e063-6394a90ac731 | 2025-12-20 | Warnings | M018 PDC6A3C0OX |
| Original Redness Reliever | TETRAHYDROLIZINE HCL | Walmart | 4414f768-0c69-d041-e063-6294a90a5bd9 | 2025-12-20 | Warnings | M018 |
| Kids Cold and Cough Daytime | CALCIUM SULFIDE,GOLDENSEAL,ONION,PHOSPHORUS,PULSATILLA VULGARIS, SODIUM CHLORIDE | Hyland's Consumer Health Inc. | e6118c79-b6d5-5c09-e053-2a95a90a30cf | 2025-12-19 | Warnings | 451W47IQ8X |
| 4 KIDS COLD N COUGH GRAPE FLAVOR | ONION, CALCIUM SULFIDE, GOLDENSEAL, SODIUM CHLORIDE, PHOSPHORUS, ANEMONE PULSATILLA, AND SULFUR | Hyland's Inc. | 798e2a4d-da2d-4bbd-a9b8-574490ef7357 | 2025-12-19 | Warnings | 451W47IQ8X |
| 4 Kids Cold and Cough Daytime | ONION, CALCIUM SULFIDE, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA VULGARIS, SULFUR, AND GOLDENSEAL | Hyland's Inc. | 804e0e7a-20eb-128b-e053-2991aa0aa82c | 2025-12-19 | Warnings | 451W47IQ8X |
| 4 Kids Cold and Cough Nighttime Natural Grape Flavor | ONION,ANEMONE PULSATILLA, PHOSPHORUS, GOLDENSEAL, CALCIUM SULFIDE, SODIUM CHLORIDE, SULFUR, MATRICARIA CHAMOMILLA AND ARABICA COFFEE BEAN | Hyland's Inc. | 7923e59a-f62c-44df-e053-2991aa0afc1e | 2025-12-19 | Warnings | 451W47IQ8X |
| Sanitizing Wipes | BENZALKONIUM CHLORIDE | Wipes LLC | 9e9a76d9-23e0-4d3a-9903-8bf7aba54aa3 | 2025-12-19 | Warnings | F5UM2KM3W7 |
| Naughty Kitty Kat | NO GAG DEEP THROAT SPRAY | INKED SUGAR, INC | 170eb644-c72c-5744-e063-6394a90a767d | 2025-12-19 | Warnings | PDC6A3C0OX |
| Walgreens Lubricant | POLYETHYLENE GLYCOL 400, AND PROPYLENE GLYCOL | Walgreens | 21dfe061-4538-2061-e063-6394a90a6e73 | 2025-12-19 | Warnings | M018 B697894SGQ |
| Artificial Tears | GLYCERIN | Geri-Care Pharmaceuticals, Corp | 7cc437e3-bad9-59be-e053-2991aa0a1da3 | 2025-12-19 | Warnings | M018 259581 B697894SGQ PDC6A3C0OX 3NXW29V3WO |
| Signature Care Eye Drops Redness and Dry Eye Relief | GLYCERIN, NAPHAZOLINE HYDROCHLORIDE | Better Living Brands LLC | 901f3bbe-e1bb-4e44-879c-711e59813a7f | 2025-12-19 | Warnings | M018 PDC6A3C0OX |
| Sterile Cord Blood Collection Unit (MSC128D) | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE SOLUTION | Maco Productions | 251fd4cb-4aa4-4473-9f89-968da856eb77 | 2025-12-18 | Warnings | 1Q73Q2JULR |
| Hair and Nail Tonic | AVENA, DNA, ELAEIS, GLANDULA SUPRARENALIS SUIS, HAMAMELIS, HEPAR SUIS, KALI SULPH, NAT MUR, NICOTINAMIDUM, PHOSPHORICUM AC, PITUITARUM POSTERIUM, RIBOFLAVINUM, THIAMINUM HYDROCHLORICUM, THUJA OCC, THYROIDINUM, URTICA UR. | Eight and Company L.L.C | 35bda785-b3a7-4928-aaea-27bf9fb6abb5 | 2025-12-18 | Warnings | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.