NDC 81179-004 - Severe DayTime NightTime Cold and Flu Relief Max Strength
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
- 81179-004
- Package NDCs from labels
- 81179-004-00
- Manufacturer
- YET HEALTH GROUP LLC
- Effective date
- 2024-01-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Severe DayTime NightTime Cold and Flu Relief Max Strength - YET HEALTH GROUP LLC | YET HEALTH GROUP LLC | 2024-01-03 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81179-004-00 | Severe DayTime NightTime Cold and Flu ReliefMax Strength | 1 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 40 | 5 mg | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 81179-004 | SEVERE DAYTIME NIGHTTIME COLD AND FLU RELIEF MAX STRENGTH (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL, GUAIFENESIN) KIT [YET HEALTH GROUP LLC] | 6 | Unmatched | 20240104_cc33f772-a42b-0c11-e053-2995a90a7a23.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.