NDC 63029-926 - SleepEze minis
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
- 63029-926
- Package NDCs from labels
- 63029-926-16
- Manufacturer
- Medtech Products Inc.
- Effective date
- 2024-01-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SleepEze 50 mg Minis_Export only 63029-926-16 | Medtech Products Inc. | 2024-01-18 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63029-926-16 | 2026-01-29 | C162847 | 48780-1 | 49896155-a95c-586f-e063-e6dba90add90 | SleepEze 50 mg Minis_Export only 63029-926-16 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63029-926-16 | SleepEze minis | 16 in 1 BOTTLE | TABLET | 16 | 2 | |
| 63029-926-16 | SleepEze minis | 1 in 1 CARTON | TABLET | 1 | 2 |
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.