Alka Seltzer Plus Maximum Strength Sinus, Allergy And Cough Power Max Gels Capsule, Liquid Filled
NDC Package 0280-0097-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Alka Seltzer Plus Maximum Strength Sinus, Allergy And Cough Power Max Gels (acetaminophen, dextromethorphan hydrobromide , doxylamine succinate, phenylephrine hydrochloride) capsules is uses · temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: · runny nose · sneezing · itching of the nose or throat · itchy, watery eyes· temporarily relieves these symptoms due to a cold: · minor aches and pains · headache · cough · sore throat · nasal congestion · sinus congestion and pressure · temporarily reduces fever. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Bayer Healthcare Llc., this product is identified by NDC 0280-0097 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
0280-0097-01
Package Description
2 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code
0280-0097
11-Digit Billing Format
00280009701
RxNorm Crosswalk
  • 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
  • RxCUI: 1297288 - APAP 325 MG / Dextromethorphan Hydrobromide 10 MG / doxylamine succinate 6.25 MG / Phenylephrine Hydrochloride 5 MG Oral Capsule

Clinical Specifications

Proprietary Name
Alka Seltzer Plus Maximum Strength Sinus, Allergy And Cough Power Max Gels
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide , Doxylamine Succinate, Phenylephrine Hydrochloride
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide; Doxylamine Succinate; Phenylephrine Hydrochloride
Dosage Form
Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Uses · temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: · runny nose · sneezing · itching of the nose or throat · itchy, watery eyes· temporarily relieves these symptoms due to a cold: · minor aches and pains · headache · cough · sore throat · nasal congestion · sinus congestion and pressure · temporarily reduces fever

Regulatory & Marketing

Labeler Name
Bayer Healthcare Llc.
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-25-2021
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 (0280-0097). Click a package code to view its specific billing and regulatory data.

0280-0097-02
2 BLISTER PACK in 1 CARTON / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

* 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 0280-0097-01 identifies a specific commercial package of 2 blister pack in 1 carton / 8 capsule, liquid filled in 1 blister pack of Alka Seltzer Plus Maximum Strength Sinus, Allergy And Cough Power Max Gels, a human over the counter drug labeled by Bayer Healthcare Llc.. This capsule, liquid filled is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide; doxylamine succinate; phenylephrine hydrochloride 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 May 25, 2021. 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: 00280009701. 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:

10-Digit Format (4-4-2)
0280-0097-01
11-Digit CMS (5-4-2)
00280-0097-01

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.