NDC 69676-0094 - Daytime and Nighttime Severe Cold and Flu combo pack
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
- 69676-0094
- Package NDCs from labels
- 69676-0094-9
- Manufacturer
- Genexa Inc.
- Effective date
- 2025-12-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Daytime and Nighttime Severe Cold & Flu Combo pack | Genexa Inc. | 2025-12-30 | HUMAN OTC DRUG LABEL |
| Cough and Chest Congestion Maximum Strength - Genexa Inc. | Genexa Inc. | 2025-07-02 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69676-0094-9 | Daytime and Nighttime Severe Cold and Flu combo pack | 177 mL in 1 BOTTLE | SUSPENSION | 177 mL | 650 mg in 20mL | 2 |
| 69676-0094-9 | Maximum Strength Cough and Chest Congestion and Nighttime Severe Cold and Flu Combo pack | 177 mL in 1 BOTTLE | SUSPENSION | 177 mL | 650 mg in 20mL | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69676-0094 | DAYTIME AND NIGHTTIME SEVERE COLD AND FLU COMBO PACK (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE) KIT [GENEXA INC.] | 1 | Unmatched | 20240927_190c7eaf-dcd4-d314-e063-6294a90a6f33.zip |
| 69676-0094 | MAXIMUM STRENGTH COUGH AND CHEST CONGESTION AND NIGHTTIME SEVERE COLD AND FLU COMBO PACK (DEXTROMETHORPHAN HBR, GUAIFENESIN, ACETAMINOPHEN, DOXYLAMINE SUCCINATE) KIT [GENEXA INC.] | 1 | Unmatched | 20240905_18835205-a9e3-15c2-e063-6394a90a8107.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.