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
- 2026-12-31
- 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
- 2026-12-31
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 |
|---|---|---|---|---|---|---|
| Walmart | ISOPROPYL ALCOHOL | Walmart, Inc. | 2eff98ba-5736-b07e-e063-6394a90aeea9 | 2026-09-04 | Warnings | M003 |
| Walgreen Alcohol | ISOPROPYL ALCOHOL | Walgreens Company | deeae1ea-3d81-4260-95be-c4f328e3fdef | 2026-09-04 | Warnings | M003 |
| Dollar General | ISOPROPYL ALCOHOL | Dollar General Corporation | 00b2ef34-42d9-523c-e063-6294a90a753d | 2026-09-03 | Warnings | M003 |
| Signature Select Alcohol Prep Pads | ISOPROPYL ALCOHOL | Better Living Brands LLC | 31ce72e3-03a3-1608-e063-6394a90ad850 | 2026-09-03 | Warnings | M003 |
| SurviveX Sting Relief | STING RELIEF WIPE | Changzhou Maokang Medical Products Co., Ltd. | 5a83b1f1-c8dc-cf07-e063-6394a90a20ca | 2026-09-03 | Warnings | M003 |
| Benzethonium chloride Plus Dyclonine hydrochloride | LIQUID BANDAGE | Kroger Co. | fe604470-917f-4cbd-a1e6-ac1dc7c57ff6 | 2026-09-02 | Warnings | M003 |
| Alcohol | ISOPROPYL ALCOHOL | Rite Aid Corporation | 5104f9ab-0b28-449f-a55a-5438713a24df | 2026-09-02 | Warnings | M003 |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | UpLift Brands, LLC | 5a81b635-d188-0b29-e063-6294a90a1e4b | 2026-09-02 | Warnings, Adverse reactions | M003 |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | CVS Pharmacy, Inc. | 7f518646-c8fe-499a-b5e4-8e5a5a90e01d | 2026-09-02 | Warnings, Adverse reactions | M003 |
| Alcohol | ISOPROPYL ALCOHOL | The Kroger Company | 6551187f-5cde-4149-931f-b057bd760750 | 2026-09-02 | Warnings | M003 |
| Unscented NasalGuard Antiseptic Topical | BENZALKONIUM CHLORIDE | TRUTEK CORP. | eb036e11-a28c-fdc0-e053-2a95a90a9cdb | 2026-09-02 | Warnings | M003 |
| Harris Teeter | ISOPROPYL ALCOHOL | Harris Teeter, LLC | d2bb20bd-ec83-8d80-e053-2a95a90a2bba | 2026-09-02 | Warnings | M003 |
| School Health | ISOPROPYL ALCOHOL | School Health Corporation | db5d0b22-f2d7-23e5-e053-2a95a90aeb51 | 2026-09-02 | Warnings | M003 |
| Alcohol Prep Pads | ISOPROPYL ALCOHOL | Topco Associates | 2642298f-607e-fdca-e063-6394a90a69d9 | 2026-09-02 | Warnings | M003 |
| HUSTLE BUTTER NUMBING | LIDOCAINE HCL, BENZALKONIUM CHLORIDE | H.B.D. DIST. INC. | 5b4d0390-dac6-4a71-9fdc-5c31543e7c5a | 2026-09-02 | Warnings | M003 |
| NasalGuard Antiseptic Topical Cool Menthol | BENZALKONIUM CHLORIDE | TRUTEK CORP. | e9fd3ef8-78ff-6c9f-e053-2a95a90a21a8 | 2026-09-01 | Warnings | M003 |
| Maximum Strength Betadine Clear | BENZALKONIUM CL AND PRAMOXINE HCL | Atlantis Consumer Healthcare, Inc. | 31b94a76-1536-47c0-ab03-e487c2625c58 | 2026-08-31 | Warnings | M003 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 5a28101f-ea8e-6071-e063-6294a90aad91 | 2026-08-31 | Warnings | M003 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 5a3e62ce-52dc-121b-e063-6294a90a898f | 2026-08-31 | Warnings | M003 |
| Biopure Antibacterial Hand Wipe | ANTIBACTERIAL HAND WIPE | Fujian Yifa Healthcare Products Co., Ltd. | 5a49db18-c270-6f46-e063-6294a90afb5d | 2026-08-31 | 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 |