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United States· US:0280-0055_45261b62-142d-8c69-e063-6294a90a011f

Alka-Seltzer Plus Maximum Strength Sinus Congestion and Pain PowerFast Fizz

A medicinal product containing chlorpheniramine maleate; phenylephrine hydrochloride; dextromethorphan hydrobromide; acetaminophen, registered in United States by Bayer HealthCare LLC..

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedAlka-Seltzer Plus Maximum Strength Si…ATC—REGISTER NO.US:0280-0055_45261b62…PACKS LISTED4CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN
Manufacturer
Bayer HealthCare LLC.
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 4

  • ndc11
    0280-0055-01
  • ndc11
    0280-0055-02
  • ndc11
    0280005501
    10 POUCH in 1 CARTON (0280-0055-01) / 2 TABLET, EFFERVESCENT in 1 POUCH
  • ndc11
    0280005502
    12 POUCH in 1 CARTON (0280-0055-02) / 2 TABLET, EFFERVESCENT in 1 POUCH

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Chlorpheniramine maleate; phenylephrine hydrochloride; dextromethorphan hydrobromide; acetaminophen in 1 other country

What each register calls a product with the same active substance — salts and hydrates count as the same.

All chlorpheniramine maleate; phenylephrine hydrochloride; dextromethorphan hydrobromide; acetaminophen products

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/e40fbd35-06ea-43ac-8d89-049bc1444ff7
GET /v1/drugs/e40fbd35-06ea-43ac-8d89-049bc1444ff7?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "2; 5; 10; 325",
  "substance": "CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN",
  "productndc": "0280-0055",
  "dosage_form": "TABLET, EFFERVESCENT",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1; mg/1; mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about chlorpheniramine maleate; phenylephrine hydrochloride; dextromethorphan hydrobromide; acetaminophen.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.