NDC 73660-003-01 - FLAVON WHITE MINT TOOTH
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
- 73660-003
- Requested NDC
- 73660-003-01
- Package NDCs from labels
- 73660-003-01, 73660-003-02
- Manufacturer
- BS and Co. Ltd | BIOSTECH CO., LTD.
- Effective date
- 2020-07-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FLAVON WHITE MINT TOOTH - BS and Co. Ltd | BIOSTECH CO., LTD. | BS and Co. Ltd | BIOSTECH CO., LTD. | 2020-07-25 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73660-003-02 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a4f1-d8a0-e053-dadaa90a6e4e | c57f91dd-19f2-404e-a4d7-dd47a0c505fd |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73660-003-01 | FLAVON WHITE MINT TOOTH | 50 g in 1 BOTTLE | POWDER, DENTIFRICE | 50 | 1 | |
| 73660-003-02 | FLAVON WHITE MINT TOOTH | 1 in 1 CARTON | POWDER, DENTIFRICE | 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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.