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 |
|---|---|---|---|---|---|---|
| Unscented NasalGuard Antiseptic Topical | BENZALKONIUM CHLORIDE | TRUTEK CORP. | eb036e11-a28c-fdc0-e053-2a95a90a9cdb | 2026-09-02 | Warnings | F5UM2KM3W7 |
| HUSTLE BUTTER NUMBING | LIDOCAINE HCL, BENZALKONIUM CHLORIDE | H.B.D. DIST. INC. | 5b4d0390-dac6-4a71-9fdc-5c31543e7c5a | 2026-09-02 | Warnings | F5UM2KM3W7 |
| Adrenal Support | ADRENALINUM, ARGENTUM NITRICUM, BERBERIS VULGARIS, NATRUM MURIATICUM, OLEUM MORRHUAE, PETROLEUM, VANADIUM | NaturalCare | 31a5d522-15cd-432a-bf87-f721bcbe2e31 | 2026-09-02 | Warnings | 451W47IQ8X |
| Xtreme Saline Rinse Mix | SODIUM BICARBONATE, SODIUM CHLORIDE | Xtreme Personal Care Inc | 776f417e-e443-4918-8c7a-1913b7dddcd4 | 2026-09-01 | Warnings | 451W47IQ8X |
| Pharmlitalia Vaginal Symptoms Relief | BORAX,CALENDULA OFFICINALIS,HYDRASTIS CANADENSIS,OLIVE EXTRACT | Guangzhou Trading Financing Union LLC | ad63f5aa-dfa7-4773-bec2-12ccf8181f95 | 2026-09-01 | Warnings | 91MBZ8H3QO |
| NasalGuard Antiseptic Topical Cool Menthol | BENZALKONIUM CHLORIDE | TRUTEK CORP. | e9fd3ef8-78ff-6c9f-e053-2a95a90a21a8 | 2026-09-01 | Warnings | F5UM2KM3W7 |
| Maximum Strength Betadine Clear | BENZALKONIUM CL AND PRAMOXINE HCL | Atlantis Consumer Healthcare, Inc. | 31b94a76-1536-47c0-ab03-e487c2625c58 | 2026-08-31 | Warnings | F5UM2KM3W7 |
| Swisher Advanced Antibacterial Foam Handsoap | BENZALKONIUM CHLORIDE | Ecolab Inc. | 38bd6680-db95-424c-8e84-2e12c2388a73 | 2026-08-31 | Warnings | F5UM2KM3W7 |
| Orajel 4X Medicated Toothache and Gum Cream | BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE | Church & Dwight Co., Inc. | 5a1c82b4-02b3-d456-e063-6294a90a16bb | 2026-08-31 | Warnings | F5UM2KM3W7 |
| Orajel 4X Medicated Toothache and Gum PM Cream | BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE | Church & Dwight Co., Inc. | 5a1cdaf4-3388-280c-e063-6294a90ac70f | 2026-08-31 | Warnings | F5UM2KM3W7 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 5a28101f-ea8e-6071-e063-6294a90aad91 | 2026-08-31 | Warnings | F5UM2KM3W7 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 5a3e62ce-52dc-121b-e063-6294a90a898f | 2026-08-31 | Warnings | F5UM2KM3W7 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 5a49db18-c270-6f46-e063-6294a90afb5d | 2026-08-31 | Warnings | F5UM2KM3W7 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 5a4ac18e-8ba5-bef6-e063-6394a90a8811 | 2026-08-31 | Warnings | F5UM2KM3W7 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 5a4d11fa-3f65-b41f-e063-6394a90a30ae | 2026-08-31 | Warnings | F5UM2KM3W7 |
| Nacl 0.9% Normal Saline Solution | SODIUM CHLORIDE | CHI FUNG TECHNOLOGY COMPANY | 5a53c4c8-c9de-700c-e063-6394a90a3ab5 | 2026-08-31 | Warnings | 451W47IQ8X |
| BMNP Kali Mur | KALIUM MURIATICUM | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 5a546950-3f03-7abf-e063-6294a90a1968 | 2026-08-31 | Warnings | 660YQ98I10 |
| BMNP Nat Mur | NATRUM MURIATICUM | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 5a57ccfd-ab6f-cb2c-e063-6394a90ae9e6 | 2026-08-31 | Warnings | 451W47IQ8X |
| Orajel 4X Medicated Toothache and Gum | BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE | Church & Dwight Co., Inc. | 5a1b4133-0eac-2f8f-e063-6394a90af8f6 | 2026-08-28 | Warnings | F5UM2KM3W7 |
| REFRESH LIQUIGEL | CARBOXYMETHYLCELLULOSE SODIUM | Allergan, Inc. | 4b8b2f6a-4b89-446c-9e5b-9b83c453a01d | 2026-08-28 | Warnings | M018 K679OBS311 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.