NDC 63029-925 - Sleepeze eze melts
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
- 63029-925
- Package NDCs from labels
- 63029-925-16
- 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 eze melts_Export only 63029-925-16 | Medtech Products Inc. | 2024-01-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63029-925-16 | Sleepeze eze melts | 1 in 1 CARTON | TABLET | 1 | 2 | |
| 63029-925-16 | Sleepeze eze melts | 8 in 1 BLISTER PACK | TABLET | 8 | 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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| Alka-Seltzer Gold | ALKA-SELTZER GOLD | Bayer HealthCare LLC. | 0824bedb-413b-2fa0-e054-00144ff88e88 | 2025-12-04 | Warnings | 2968PHW8QP |
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| Nighttime Sleep-Aid | DIPHENHYDRAMINE HCL | BIONPHARMA INC. | 1f74e760-9ba9-ac47-e063-6394a90acdff | 2025-12-01 | Warnings | TC2D6JAD40 |
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| Allergy Relief | DIPHENHYDRAMINE HCL | BIONPHARMA INC. | 323347c3-d51a-4976-e063-6294a90a952e | 2025-12-01 | Warnings | TC2D6JAD40 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.