NDC 70000-0705-01 - Leader Lubricant Eye Drops Soothing Relief
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
- 70000-0705
- Requested NDC
- 70000-0705-01
- Package NDCs from labels
- 70000-0705-1, 70000-0705-2, 70000-0705-01
- Manufacturer
- LEADER/Cardinal Health 110, Inc. | KC Pharmaceuticals, Inc.
- Effective date
- 2025-12-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Leader Lubricant Eye Drops Soothing Relief 15mL & 15mL twin pk (PLD) | LEADER/Cardinal Health 110, Inc. | KC Pharmaceuticals, Inc. | 2025-12-30 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70000-0705-1 | Leader Lubricant Eye Drops Soothing Relief | 1 in 1 BOX | SOLUTION/ DROPS | 1 | 3 | |
| 70000-0705-1 | Leader Lubricant Eye Drops Soothing Relief | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | 3 | |
| 70000-0705-2 | Leader Lubricant Eye Drops Soothing Relief | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | 3 | |
| 70000-0705-2 | Leader Lubricant Eye Drops Soothing Relief | 2 in 1 BOX | SOLUTION/ DROPS | 2 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70000-0705 | LEADER LUBRICANT EYE DROPS SOOTHING RELIEF (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [LEADER/CARDINAL HEALTH 110, INC.] | 2 | Current NDC, 4 package rows | 20241008_218629d4-2704-a503-e063-6294a90a3953.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70000-0705-1 | ML - Milliliter | 70000-0705 | f2ff4e8b-ecee-4792-a05e-275bcff544c8 | 1 | 2025-08-11 |
| 70000-0705-2 | ML - Milliliter | 70000-0705 | 502e3738-ffa1-4b23-9a0e-ed96ce93ea90 | 1 | 2025-09-12 |
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 |
|---|---|---|---|---|---|---|
| Family Beauty Antibacterial Hand Wipes | BENZALKONIUM CHLORIDE | Zhejiang Bright Care Co., Ltd. | 6ff604f7-4011-4f0e-aa2d-a46e1a973d13 | 2026-08-21 | Warnings | F5UM2KM3W7 |
| Potassium Chloride | POTASSIUM CHLORIDE | Coupler LLC | 598f61d7-a665-5d02-e063-6394a90a8905 | 2026-08-21 | Warnings, Adverse reactions | 660YQ98I10 |
| Softsoap Antibacterial Clean and Protect Cool Splash | BENZALKONIUM CHLORIDE | COLGATE PALMOLIVE COMPANY | 7d48e018-0874-4bbf-a95e-dc21702406c1 | 2026-08-20 | Warnings | F5UM2KM3W7 |
| Rohto Optic Glow | NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff | 2026-08-20 | Warnings | M018 |
| Rohto All-In-One | HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE | The Mentholatum Company | 43e690e4-b381-46e3-838c-33aef5bdadde | 2026-08-20 | Warnings | M018 |
| Rohto Max Strength | NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80 | The Mentholatum Company | e4b49550-1ca3-4bd7-854d-409b53fa5e26 | 2026-08-20 | Warnings | M018 |
| Bio Combination 28 | SCHUESSLER SALTS | LDD Bioscience Private Limited | 597caf33-5107-9dec-e063-6294a90a5fcd | 2026-08-20 | Warnings | 451W47IQ8X 660YQ98I10 |
| Olimpo Antibacterial | BENZALKONIUM CHLORIDE 0.1% | Industria La Popular, S.A. | 597e3b3e-51f0-5fcf-e063-6394a90ac297 | 2026-08-20 | Warnings | F5UM2KM3W7 |
| Sodium Chloride | SODIUM CHLORIDE | YYBA CORP | 597f3347-647c-3545-e063-6294a90abab2 | 2026-08-20 | Warnings | M018 451W47IQ8X |
| Benzalkonium Chloride | BENZALKONIUM CHLORIDE TOWELETTES | Trifecta Pharmaceuticals USA LLC | 59811e67-57f0-4db1-e063-6294a90a2ad8 | 2026-08-20 | Warnings | F5UM2KM3W7 |
| Sodium Chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | 2e5fe9f4-78e5-4af4-8bf9-9680e5dc5e88 | 2026-08-20 | Warnings, Adverse reactions | 451W47IQ8X |
| Sinusforce-HP | ARSENICUM ALBUM, HEPAR SULPHURIS CALCAREUM, KALI BICHROMICUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SEPIA | BioActive Nutritional, Inc. | 53c96680-210b-4426-8b41-3b9a882848dd | 2026-08-20 | Warnings | 451W47IQ8X |
| CVS Saline | NASAL | CVS PHARMACY | f02c41b0-c78e-41cd-aa4a-2756bbe92087 | 2026-08-19 | Warnings | 451W47IQ8X |
| Mineral Oil/White Petrolatum | MINERAL OIL/WHITE PETROLATUM | YYBA CORP | 5967ef02-6770-bfd7-e063-6294a90a7904 | 2026-08-19 | Warnings | M018 |
| Dextrose and Sodium Chloride | DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE | Fresenius Kabi USA, LLC | df18a603-ca12-4b26-83b5-9dd07b6453ab | 2026-08-18 | Warnings, Adverse reactions | 451W47IQ8X |
| DELFLEX | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE | Fresenius Medical Care Renal Therapies Group, LLC | bbc5b820-4973-11e2-a192-0002a5d5c51b | 2026-08-18 | Warnings, Adverse reactions | 02F3473H9O 451W47IQ8X |
| DELFLEX | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE | Fresenius Medical Care Renal Therapies Group, LLC | c29bdfa0-4976-11e2-939b-0002a5d5c51b | 2026-08-18 | Warnings, Adverse reactions | 02F3473H9O 451W47IQ8X |
| DELFLEX | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE | Fresenius Medical Care Renal Therapies Group, LLC | 515dcee0-3e34-11e2-a25f-0800200c9a66 | 2026-08-18 | Warnings, Adverse reactions | 02F3473H9O 451W47IQ8X |
| Rohto Preservative Free Dry Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | f4b1974c-2412-45f6-b79d-88b8a0bcb608 | 2026-08-18 | Warnings | M018 |
| Rohto Dry-Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | 8ea5c6c9-48f4-406a-a2cb-9280c546d87d | 2026-08-18 | Warnings | M018 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.