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United States· US:0280-1640_45268308-4951-be8f-e063-6394a90a9343

Alka-Seltzer Plus Maximum Strength Night Cold and Flu PowerMax Gels

A medicinal product containing phenylephrine hydrochloride; acetaminophen; dextromethorphan hydrobromide; doxylamine succinate, 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 Ni…ATC—REGISTER NO.US:0280-1640_45268308…PACKS LISTED4CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
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
    0280164016
    2 BLISTER PACK in 1 CARTON (0280-1640-16) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • ndc11
    0280164024
    3 BLISTER PACK in 1 CARTON (0280-1640-24) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • ndc11
    0280-1640-16
  • ndc11
    0280-1640-24

Regulatory notes

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

Same medicine, other countries

Phenylephrine hydrochloride; acetaminophen; dextromethorphan hydrobromide; doxylamine succinate in 1 other country

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

All phenylephrine hydrochloride; acetaminophen; dextromethorphan hydrobromide; doxylamine succinate 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/0bfbcd51-0cc7-4fe2-a2c1-74b611ddcf65
GET /v1/drugs/0bfbcd51-0cc7-4fe2-a2c1-74b611ddcf65?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": "5; 325; 10; 6.25",
  "substance": "PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE",
  "productndc": "0280-1640",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1; mg/1; mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about phenylephrine hydrochloride; acetaminophen; dextromethorphan hydrobromide; doxylamine succinate.

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.