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United States· US:50580-584_4e60e1ad-4ad5-c329-e063-6294a90ab318

Tylenol Cold Plus Flu Plus Chest Congestion

A medicinal product containing guaifenesin; acetaminophen, registered in United States by Kenvue Brands 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…normalisedTylenol Cold Plus Flu Plus Chest Cong…ATC—REGISTER NO.US:50580-584_4e60e1ad…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
GUAIFENESIN; ACETAMINOPHEN
Manufacturer
Kenvue Brands 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 · 2

  • ndc11
    5058058424
    2 BLISTER PACK in 1 CARTON (50580-584-24) / 12 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    50580-584-24

Regulatory notes

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

Same medicine, other countries

Guaifenesin; acetaminophen in 1 other country

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

All guaifenesin; acetaminophen products

Authorised across Europe · EMA

The same active substance is authorised in 1 EEA country. Names it is sold under:

  • Ireland · Lemsip Max Cough & Cold

Source: European Medicines Agency, Article 57 product data.

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/12aa90a6-817c-40f1-8075-76953dbc1d6f
GET /v1/drugs/12aa90a6-817c-40f1-8075-76953dbc1d6f?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": "200; 325",
  "substance": "GUAIFENESIN; ACETAMINOPHEN",
  "productndc": "50580-584",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about guaifenesin; 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.