NDC 72863-101-01 - Himalayan Pink Salt Sweet Herbal Mint
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
- 72863-101
- Requested NDC
- 72863-101-01
- Package NDCs from labels
- 72863-101-01, 72863-101-02
- Manufacturer
- Rael, Inc. | Sangleaf Pharm., Co Ltd
- Effective date
- 2019-02-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Himalayan Pink Salt Sweet Herbal Mint - Rael, Inc. | Sangleaf Pharm., Co Ltd | Rael, Inc. | Sangleaf Pharm., Co Ltd | 2019-02-28 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72863-101-02 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-3295-f274-e053-dbdaa90a6471 | Himalayan Pink Salt Toothpaste (Sweet Herbal Mint) |
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 |
|---|---|---|---|---|---|---|
| FLUORIDEX | SODIUM FLUORIDE | DEN-MAT HOLDINGS, LLC. | 5fd60635-4b66-15e3-e053-2991aa0ab23a | 2019-02-28 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Pro-Den Rx | SODIUM FLUORIDE | Den-mat Holdings, Llc | e39b19f7-2b3e-4c77-9544-623ebad84870 | 2019-02-28 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| FLUORIDEX | SODIUM FLUORIDE | DEN-MAT HOLDINGS, LLC. | 6014c330-3698-027c-e053-2a91aa0a64e5 | 2019-02-28 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Plus White | SODIUM MONOFLUOROPHOSPHATE | CCA Industries, Inc. | 7581b27b-6acb-45b0-8804-b5dae3498931 | 2018-08-01 | Warnings | C810JCZ56Q |
| Pro-Den Rx | SODIUM FLUORIDE | Den-Mat Holdings, Llc | ba020e07-ad41-4419-a503-f1245131b7d2 | 2018-04-17 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Sensitive Tooth Polish | POTASSIUM NITRATE AND SODIUM FLUORIDE | Melaleuca, Inc. | 689349e4-3980-a0e4-e053-2991aa0a9ef5 | 2018-03-29 | Warnings | 8ZYQ1474W7 |
| SF | 1.1% SODIUM FLUORIDE | Cypress Pharmaceutical, Inc. | b7c0a768-7e8a-40b9-876f-b86d3dc5e848 | 2016-07-06 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| SF 5000 Plus | 1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM | Cypress Pharmaceutical, Inc. | fa625ece-d873-491a-8d45-2833b64e5425 | 2016-07-01 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Ionite H | SODIUM FLUORIDE, POTASSIUM NITRATE | Dharma Research, Inc. | 54c1a27c-5936-4ee2-a419-3891d3df9745 | 2015-08-02 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Ionite H | SODIUM FLUORIDE, POTASSIUM NITRATE | Dharma Research, Inc. | 642fec99-c5c5-4ef2-986e-5b5f7cf460de | 2015-08-02 | Warnings, Adverse reactions | 8ZYQ1474W7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.