NDC 11673-540 - daytime severe cold and cough and nighttime severe cold and cough
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
- 11673-540
- Package NDCs from labels
- 11673-540-06
- Manufacturer
- Target Corporation
- Effective date
- 2018-01-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| daytime severe cold and cough - Target Corporation | Target Corporation | 2018-01-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11673-540-06 | daytime severe cold and cough and nighttime severe cold and cough | 6 in 1 CARTON | POWDER, FOR SOLUTION | 6 | 20 mg | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11673-540 | DAYTIME SEVERE COLD AND COUGH AND NIGHTTIME SEVERE COLD AND COUGH (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL) KIT [TARGET CORPORATION] | 1 | Unmatched | 20180123_62eec235-431f-4429-b173-d4a9b45a4e36.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.