Alka Seltzer Cold Cold Flu And Congestion Maximum Strength Day Night Fast Gels Kit
NDC Package 0280-8288-24
Package Information
Alka Seltzer Cold Cold Flu And Congestion Maximum Strength Day Night Fast Gels (acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, doxylamine succinate) kits is uses · temporarily relieves these symptoms due to a cold or flu:· minor aches and pains · headache· cough · sore throat· sinus congestion and pressure · nasal congestion· temporarily reduces fever. This formulation utilizes a kit delivery system. Marketed by Bayer Healthcare Llc., this product is identified by NDC 0280-8288 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
- RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
- RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
- RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Capsule
- RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Capsule
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0280 - Bayer Healthcare Llc.
- 0280-8288 - Alka Seltzer Cold Cold Flu And Congestion Maximum Strength Day Night Fast Gels
- 0280-8288-24 - 1 KIT in 1 CARTON * 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
- 0280-8288 - Alka Seltzer Cold Cold Flu And Congestion Maximum Strength Day Night Fast Gels
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (0280-8288). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0280-8288-24 identifies a specific commercial package of 1 kit in 1 carton * 1 capsule, liquid filled in 1 blister pack * 1 capsule, liquid filled in 1 blister pack * 1 capsule, liquid filled in 1 blister pack * 1 capsule, liquid filled in 1 blister pack of Alka Seltzer Cold Cold Flu And Congestion Maximum Strength Day Night Fast Gels, a human over the counter drug labeled by Bayer Healthcare Llc.. This kit is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Bayer Healthcare Llc. on June 01, 2026. The current certification is valid through December 31, 2027.
How is this Bayer Healthcare Llc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00280828824. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.
