NDC 69842-290 - MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS 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
- 69842-290
- Package NDCs from labels
- 69842-290-08
- Manufacturer
- CVS Pharmacy, Inc. | TIME CAP LABORATORIES, INC. | MARKSANS PHARMA LIMITED
- Effective date
- 2026-03-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 630T CVS 69842-442 MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEF | CVS Pharmacy, Inc. | TIME CAP LABORATORIES, INC. | MARKSANS PHARMA LIMITED | 2026-03-26 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69842-290-08 | MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEF | 8 in 1 BLISTER PACK | CAPSULE, LIQUID FILLED | 8 | 6.25 mg | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69842-290 | MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEF (ACETAMINOPHEN DEXTROMETHORPHAN HBR GUAIFENESIN PHENYLEPHRINE HCL AND ACETAMINOPHEN DEXTROMETHORPHAN HBR DOXYLAMINE SUCCINATE PHENYLEPHRINE HCL) KIT [CVS PHARMACY, INC.] | 3 | Unmatched | 20250215_c17d5ba7-3302-7931-e053-2a95a90a5a6c.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.