ALKA SELTZER COLD Cold Flu Congestion Severe Fast Hot Liquid Day Night
- Product NDC
- 0280-8284
- 11-digit product format
- 002808284
- Labeler code
- 0280
- Product ID
- 0280-8284_53715ea4-42b4-5887-e063-6294a90a4249
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan hydrobromide, Guaifenesin, Phenylephrine hydrochloride, and Doxylamine succinate
- Dosage form
- KIT
- Labeler
- Bayer HealthCare LLC.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-01
- 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
- ALKA SELTZER COLD Cold Flu Congestion Severe Fast Hot Liquid Day Night
- Listing expiration
- 2027-12-31
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 53715ea4-42b3-5887-e063-6294a90a4249 | Available on FDA.report |
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 |
|---|---|---|---|---|---|---|---|
| 0280-8284-12 | 00280828412 | 1 KIT in 1 CARTON (0280-8284-12) * 1 POWDER, FOR SOLUTION in 1 PACKET * 1 POWDER, FOR SOLUTION in 1 PACKET | 1 kit | 2026-06-01 | No | No | Current |