NDC 73242-1122-01 - DOCTRUST DOUBLEX 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
- 73242-1122
- Requested NDC
- 73242-1122-01
- Package NDCs from labels
- 73242-1122-1, 73242-1122-2, 73242-1122-01
- Manufacturer
- DONG IL PHARMS CO.,LTD | DONG IL PHARMS CO., LTD.
- Effective date
- 2025-11-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DOCTRUST DOUBLEX Tooth - DONG IL PHARMS CO.,LTD | DONG IL PHARMS CO., LTD. | DONG IL PHARMS CO.,LTD | DONG IL PHARMS CO., LTD. | 2025-11-25 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73242-1122-1 | DOCTRUST DOUBLEX Tooth | 100 g in 1 TUBE | PASTE, DENTIFRICE | 100 | 1 | |
| 73242-1122-2 | DOCTRUST DOUBLEX Tooth | 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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| Crest 3D White Fresh Mint | SODIUM FLUORIDE | Procter & Gamble Manufactura, S. de R.L. de C.V. | 01f27a63-15f3-cee4-e063-6394a90afa3b | 2026-01-08 | Warnings | M021 8ZYQ1474W7 |
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| Crest Strawberry | SODIUM FLUORIDE | Procter & Gamble Manufactura, S. de R.L. de C.V. | 7d615c52-f9c9-4856-e053-2991aa0a7927 | 2026-01-08 | Warnings | M021 8ZYQ1474W7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.