NDC 73660-002-01 - FLAVON CHARCOAL 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
- 73660-002
- Requested NDC
- 73660-002-01
- Package NDCs from labels
- 73660-002-01, 73660-002-02
- 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 CHARCOAL 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 |
|---|---|---|---|---|---|
| 73660-002-02 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a881-d8a0-e053-dadaa90a6e4e | 950b8e67-c5ea-4120-b272-966f12de25dd |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73660-002-01 | FLAVON CHARCOAL MINT TOOTH | 50 g in 1 BOTTLE | POWDER, DENTIFRICE | 50 | 1 | |
| 73660-002-02 | FLAVON CHARCOAL 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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| Bactimicina Vapor Rub | VAPOR RUB | DLC Laboratories, Inc. | 176b617a-faf6-7893-e063-6294a90a046b | 2026-01-07 | Warnings | L7T10EIP3A |
| Tiger Balm Active Muscle | METHYL SALICYLATE AND MENTHOL, UNSPECIFIED FORM | Haw Par Healthcare Ltd. | 845a4ead-f9c0-4009-bcae-b17cd388439b | 2026-01-07 | Warnings | L7T10EIP3A |
| 3X Medicated Toothache and Gum Gel | BENZOCAINE | Rite Aid | 996f7989-17ce-5b28-e053-2995a90af8b8 | 2026-01-06 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.