NDC 70602-009-01 - ANABIOSE PURIHEAL
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
- 70602-009
- Requested NDC
- 70602-009-01
- Package NDCs from labels
- 70602-009-01, 70602-009-02, 70602-009-03, 70602-009-04, 70602-009-05, 70602-009-06
- Manufacturer
- LIFEON Corp. | KONAD CO LTD
- Effective date
- 2022-07-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ANABIOSE PURIHEAL - LIFEON Corp. | KONAD CO LTD | LIFEON Corp. | KONAD CO LTD | 2022-07-12 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70602-009-02 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-acdb-d83d-e063-dadaa90ab31f | 70602-009_ANABIOSE PURIHEAL SHAMPOO |
| 70602-009-04 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-acdb-d83d-e063-dadaa90ab31f | 70602-009_ANABIOSE PURIHEAL SHAMPOO |
| 70602-009-06 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-acdb-d83d-e063-dadaa90ab31f | 70602-009_ANABIOSE PURIHEAL SHAMPOO |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70602-009-01 | ANABIOSE PURIHEAL | 300 mL in 1 BOTTLE, PUMP | SHAMPOO | 300 | 1 | |
| 70602-009-02 | ANABIOSE PURIHEAL | 1 in 1 CARTON | SHAMPOO | 1 | 1 | |
| 70602-009-03 | ANABIOSE PURIHEAL | 500 mL in 1 BOTTLE, PUMP | SHAMPOO | 500 | 1 | |
| 70602-009-04 | ANABIOSE PURIHEAL | 1 in 1 CARTON | SHAMPOO | 1 | 1 | |
| 70602-009-05 | ANABIOSE PURIHEAL | 1000 mL in 1 BOTTLE, PUMP | SHAMPOO | 1000 | 1 | |
| 70602-009-06 | ANABIOSE PURIHEAL | 1 in 1 CARTON | SHAMPOO | 1 | 1 |
DailyMed Dashboard NDC Coverage#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.