NDC 81307-040-01 - Teen Toothpast e Eucalyptus Flavor
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
- 81307-040
- Requested NDC
- 81307-040-01
- Package NDCs from labels
- 81307-040-01, 81307-040-02
- Manufacturer
- MGRU | DONG IL PHARMS CO., LTD.
- Effective date
- 2020-12-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Teen Toothpast e Eucalyptus Flavor - MGRU | DONG IL PHARMS CO., LTD. | MGRU | DONG IL PHARMS CO., LTD. | 2020-12-23 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81307-040-02 | 2024-12-26 | C162847 | 48780-1 | f386c64a-3105-0266-e053-dadaa90a7c1a | 3f680211-cb2a-4c43-8c54-bbd73c585b3d |
| 81307-040-02 | 2023-01-30 | C162847 | 48780-1 | f386c64a-3105-0266-e053-dadaa90a7c1a | 3f680211-cb2a-4c43-8c54-bbd73c585b3d |
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.