Cold Flu
- Product NDC
- 42507-598
- 11-digit product format
- 425070598
- Labeler code
- 42507
- Product ID
- 42507-598_21dcb521-6f50-4d61-9b3e-92d99004bbce
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
- Dosage form
- KIT
- Labeler
- HyVee Inc
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-17
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cold Flu
- Listing expiration
- 2027-12-31
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 42507-598-02 | 42507059802 | 1 KIT in 1 CARTON (42507-598-02) * 355 mL in 1 BOTTLE (42507-811-40) * 355 mL in 1 BOTTLE (42507-532-40) | 1 kit | 2026-09-17 | No | No | Current |