NDC 11822-0710-01 - daytime nighttime severe cold and flu relief
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
- 11822-0710
- Requested NDC
- 11822-0710-01
- Package NDCs from labels
- 11822-0710-1, 11822-0710-01
- Manufacturer
- Rite Aid Corporation
- Effective date
- 2026-09-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| daytime nighttime severe cold and flu relief - Rite Aid Corporation | Rite Aid Corporation | 2026-09-10 | HUMAN OTC DRUG LABEL |
| Daytime Severe Cold and Flu Relief - Rite Aid Corporation | Rite Aid Corporation | 2026-07-24 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11822-0710-1 | Daytime Severe Cold and Flu Relief | 355 mL in 1 BOTTLE | SOLUTION | 355 | 6 | |
| 11822-0710-1 | daytime nighttime severe cold and flu relief | 355 mL in 1 BOTTLE | SOLUTION | 355 mL | 5 mg in 15mL | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11822-0710 | DAYTIME SEVERE COLD AND FLU RELIEF (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [RITE AID CORPORATION] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241030_8d41defe-8120-4cbb-b42e-c805cc5a794b.zip |
| 11822-0710 | DAYTIME NIGHTTIME SEVERE COLD AND FLU RELIEF (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [RITE AID CORPORATION] | 4 | Current NDC, Legacy NDC | 20241116_eb58871d-f351-47a1-aeab-254ec6693ddd.zip |
DailyMed Socrata Ingredients#
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.