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United States· US:72854-208_51b4e933-f056-2a27-e063-6394a90a839f

Maximum Strength Mucinex Sinus-Max Pressure, Pain and Cough

A medicinal product containing guaifenesin; acetaminophen, registered in United States by Reckitt Benckiser 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…normalisedMaximum Strength Mucinex Sinus-Max Pr…ATC—REGISTER NO.US:72854-208_51b4e933…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
GUAIFENESIN; ACETAMINOPHEN
Manufacturer
Reckitt Benckiser 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 · 8

  • ndc11
    7285420802
    2 TABLET, FILM COATED in 1 POUCH (72854-208-02)
  • ndc11
    7285420808
    4 POUCH in 1 CARTON (72854-208-08) / 2 TABLET, FILM COATED in 1 POUCH
  • ndc11
    7285420810
    1 BLISTER PACK in 1 CARTON (72854-208-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    7285420820
    2 BLISTER PACK in 1 CARTON (72854-208-20) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    72854-208-02
  • ndc11
    72854-208-08
  • ndc11
    72854-208-10
  • ndc11
    72854-208-20

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/bf9cbe79-48ab-4f0a-b4b4-6b18f19625cb
GET /v1/drugs/bf9cbe79-48ab-4f0a-b4b4-6b18f19625cb?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": "72854-208",
  "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.