LEADER 2% Mild Iodine Tincture
- Product NDC
- 70000-0401
- 11-digit product format
- 700000401
- Labeler code
- 70000
- Product ID
- 70000-0401_1855b847-f240-9f78-e063-6394a90a3df3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Iodine and Sodium Iodide and Alcohol Liquid
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Cardinal Health, 110 dba Leader
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-01-15
- Substance
- SODIUM IODIDE; IODINE
- Active strength
- 24; 20 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2024-03-11 06:39 UTC · source 2024-03-08 | excluded product | product | 70000-0401 | I | Inactivated by FDA | excluded / ndc_excluded.zip | 1332a3947898… | d4bfe170f9cd… | ||
| 2024-03-11 06:39 UTC · source 2024-03-08 | excluded package | package | 70000-0401 | 70000-0401-1 | I | Inactivated by FDA | excluded / ndc_excluded.zip | 1332a3947898… | d4bfe170f9cd… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LEADER 2% Mild Iodine Tincture
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM IODIDE | 24 mg/mL |
| IODINE | 20 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| F5WR8N145C | Internal UNII lookup |
| 9679TC07X4 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2284244 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 7f810b92-60f6-2f72-e053-2991aa0ab973 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 5f30b278-5791-4113-8781-878a9221ef8a | Product name | 2 | 20230125 |
| 2a70c781-a755-4d76-b20a-a958acfbdcdc | Product name | 2 | 20190619 |
| 304592ef-4a8a-4c22-8e8c-af73aa3d60e5 | Product name | 1 | 20180703 |
| ac0821a1-ce75-4ea7-880a-59eecaecdf22 | Product name | 1 | 20180703 |
| db5dc4f9-b907-46f6-8fb7-babcf04bbe5c | Product name | 1 | 20180619 |
| 41e9d6cf-3ed7-4c44-a57e-0685058d0896 | Product name | 1 | 20170824 |
| 5e652c92-68fd-426b-b0e7-5fc64e0b9f99 | Product name | 1 | 20170309 |
| ddc0c11a-bba8-408f-b3c7-c4828b4bcc8c | Product name | 1 | 20150421 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70000-0401-1 | 2024-05-13 | C162847 | 48780-1 | 1030e365-2ef8-111a-e063-dadaa90a10e2 | LEADER 2% Mild Iodine Tincture |
| 70000-0401-1 | 2024-01-30 | C162847 | 48780-1 | 1030e365-2ef8-111a-e063-dadaa90a10e2 | LEADER 2% Mild Iodine Tincture |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70000-0401-1 | LEADER 2% Mild Iodine Tincture | 30 mL in 1 BOTTLE, PLASTIC | LIQUID | 30 | 5 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70000-0401-1 | ML - Milliliter | 70000-0401 | 991c2419-4dc6-480a-89f9-187c53ec5be1 | 1 | 2019-08-06 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70000-0401 | LEADER 2% MILD IODINE TINCTURE (IODINE AND SODIUM IODIDE AND ALCOHOL LIQUID) LIQUID [CARDINAL HEALTH, 110 DBA LEADER] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240514_7f810b92-60f6-2f72-e053-2991aa0ab973.zip |
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 |
|---|---|---|---|---|---|---|
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | dceced03-eeb8-fced-e053-2995a90afd5c | 2025-12-06 | Warnings | M003 |
| Hand Sanitizer | HAND SANITIZER | Zhejiang Meimi Technology Co., Ltd. | dced643b-96fb-193f-e053-2a95a90a16aa | 2025-12-06 | Warnings | M003 |
| Betadine Foam Cleanser | BENZALKONIUM CHLORIDE | Atlantis Consumer Healthcare, Inc. | 3be9fa6e-3ae8-496b-876b-f81f1cd98af4 | 2025-12-05 | Warnings | M003 |
| 2XL Mega Rolls Sanitizing Wipes | BENZALKONIUM CHLORIDE | 2xl Corporation | 9da541ab-6836-4149-a86d-3b2f2e586628 | 2025-12-05 | Warnings | M003 |
| Hand Wipes | BENZALKONIUM CHLORIDE | Advanced Ultrasound Solutions Inc. | 2c2abaa8-c152-470b-a4d9-5056815a1987 | 2025-12-05 | Warnings | M003 |
| Benzalkonium Chloride | SANITIZING HAND WIPES | ALO NEW YORK LLC | d3d95355-3af7-43e3-e053-2a95a90a0fa4 | 2025-12-05 | Warnings | M003 |
| Giant Eagle Antibacterial Hand Wipes | BENZALKONIUM CHLORIDE | Giant Eagle | e20e9a93-03c3-77f8-e053-2995a90ae59f | 2025-12-05 | Warnings | M003 |
| Antibacterial Wipes | BENZALKONIUM CHLORIDE | ERC Acquisition, Inc | dc6c39af-447c-481a-98b5-33b8f09b83bc | 2025-12-05 | Warnings | M003 |
| Sanitex Antibacterial Hand Wipes Fresh Scent | BENZALKONIUM CHLORIDE | Precare Corp | 48907146-ca66-46e1-928b-a8f968a6bff8 | 2025-12-05 | Warnings | M003 |
| Benzalkonium Chloride | ANTIBACTERIAL HAND WIPES | Quest USA Corp | d9ab219d-07e3-2019-e053-2a95a90a1668 | 2025-12-05 | Warnings | M003 |
| Benzalkonium Chloride | DUAL ACTION ANTIBACTERIAL WIPES | Avro Enterprises LLC | cf42e470-19c8-2e11-e053-2995a90ae90d | 2025-12-05 | Warnings | M003 |
| Benzalkonium Chloride | DUAL ACTION ANTIMICROBIAL WIPES | Avro Enterprises LLC | cf4680f4-24b2-1242-e053-2a95a90a9374 | 2025-12-05 | Warnings | M003 |
| Benzalkonium Chloride | ANTIBACTERIAL HAND WIPES | Target Corporation | f6037707-c6bb-11a0-e053-2995a90acce8 | 2025-12-05 | Warnings | M003 |
| Sanitizing Wipes | BENZALKONIUM CHLORIDE | Zogics, LLC | 2cd916ee-dc6d-49e4-a9b5-06ad4b2b054d | 2025-12-05 | Warnings | M003 |
| GELLE-N-DETOX - LAVENDER AND ROSEMARY MASSAGE | BENZALKONIUM CHLORIDE | CHEMCO CORPORATION | f28c2c1e-7d0a-45b9-e053-2995a90a4710 | 2025-12-05 | Warnings | M003 |
| GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE | BENZALKONIUM CHLORIDE | CHEMCO CORPORATION | f2a107aa-5ad3-7bad-e053-2a95a90a1d97 | 2025-12-05 | Warnings | M003 |
| PROHEAL POVIDONE IODINE SWABSTICK | POVIDONE-IODINE | Click Industries LLC | 974e1205-01ab-4599-9229-cdf5225d268a | 2025-12-03 | Warnings | M003 |
| Smart Care Hand Sanitizer Jasmine Gardenia | ALCOHOL | Shenzhen Lantern Scicence Co.,Ltd. | 45082749-6f53-c595-e063-6294a90ac3e9 | 2025-12-03 | Warnings | M003 |
| ALCOHOL PREP PAD | 70% ISOPROPY ALCOHOL SWAB | PurCel Labs LLC | 450c39fd-d172-492e-e063-6294a90aa396 | 2025-12-03 | Warnings | M003 |
| Hand Sanitizer | HAND SANITIZER | Dynarex Corporation | 450e56f0-b8ae-072a-e063-6394a90a2d4b | 2025-12-03 | Warnings | M003 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 2284244 | iodine 2 % / sodium iodide 2.4 % Topical Solution | PSN | 7f810b92-60f6-2f72-e053-2991aa0ab973 | 5 |
| 2284244 | iodine 20 MG/ML / sodium iodide 24 MG/ML Topical Solution | SCD | 7f810b92-60f6-2f72-e053-2991aa0ab973 | 5 |
| 2284244 | iodine 2 % / sodium iodide 2.4 % Topical Solution | SY | 7f810b92-60f6-2f72-e053-2991aa0ab973 | 5 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70000-0401-1 | 70000040101 | 30 mL in 1 BOTTLE, PLASTIC (70000-0401-1) | 30 ml | 2019-01-15 | 0000-00-00 | No | No | Current |