NDC 50269-101 - THERAFLU SEVERE COLD RELIEF NIGHTTIME
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
- 50269-101
- Package NDCs from labels
- 50269-101-06
- Manufacturer
- JC World Bell Wholesale Co., Inc.
- Effective date
- 2024-05-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| THERAFLU SEVERE COLD RELIEF NIGHTTIME, Honey (Honey Lemon Flavor) | JC World Bell Wholesale Co., Inc. | 2024-05-22 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50269-101-06 | THERAFLU SEVERE COLD RELIEF NIGHTTIME | 1 in 1 PACKET | POWDER, FOR SOLUTION | 1 | 1 | |
| 50269-101-06 | THERAFLU SEVERE COLD RELIEF NIGHTTIME | 20 in 1 BOX | POWDER, FOR SOLUTION | 20 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50269-101 | THERAFLU SEVERE COLD RELIEF NIGHTTIME (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE) POWDER, FOR SOLUTION [JC WORLD BELL WHOLESALE CO., INC.] | 1 | 2 package rows | 20240523_6ee1cc52-2d7e-4b53-a0e6-563e623bcb51.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.