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.
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| RET Heart 7009 | RET HEART | Professional Complementary Health Formulas | e2bf8331-1c50-4216-93a4-1d3cf6404759 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.