NDC 78151-100-01 - KarlnHans Fresh Breath Double 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
- 78151-100
- Requested NDC
- 78151-100-01
- Package NDCs from labels
- 78151-100-01, 78151-100-02
- Manufacturer
- PIGEON CORPORATION | DONG IL PHARMS CO., LTD.
- Effective date
- 2025-06-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | PIGEON CORPORATION | DONG IL PHARMS CO., LTD. | 2025-06-23 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 78151-100-01 | KarlnHans Fresh Breath Double Mint | 120 g in 1 TUBE | PASTE, DENTIFRICE | 120 | 1 | |
| 78151-100-02 | KarlnHans Fresh Breath Double Mint | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | 1 |
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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| United Airlines Therabody UPP Kit | SODIUM MONOFLUOROPHOSPHATE | Wessco International | fb6c355b-a67d-c4b4-e053-6394a90a0e66 | 2023-10-26 | Warnings | M021 |
| United Dental Kit | SODIUM MONOFLUOROPHOSPHATE | Wessco International | 7f348fe7-9918-4934-bed0-f0a77c09d046 | 2023-10-26 | Warnings | M021 |
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| Cavity Protection Fresh Mint | SODIUM FLUORIDE | Oxyfresh Worldwide Inc | 0ae98f28-7e78-4379-93b0-4f2657415c4d | 2023-10-25 | Warnings | M021 |
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| Tanners Tasty Ooh La La Orange | SODIUM FLUORIDE | Sheffield Pharmaceuticals LLC | 6027b961-314e-4f71-8b2f-646ce80214d8 | 2023-10-24 | Warnings | M021 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.