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United States· US:72854-085_51bad8ca-7226-ecef-e063-6394a90a8fc3

Mucinex Childrens Mighty Chews Night Time Cold and Flu

A medicinal product containing dextromethorphan hydrobromide; doxylamine succinate; 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…normalisedMucinex Childrens Mighty Chews Night …ATC—REGISTER NO.US:72854-085_51bad8ca…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; 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 · 2

  • ndc11
    7285408516
    16 TABLET, CHEWABLE in 1 BOTTLE (72854-085-16)
  • ndc11
    72854-085-16

Regulatory notes

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

Same medicine, other countries

Dextromethorphan hydrobromide; doxylamine succinate; acetaminophen in 3 other countries

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

All dextromethorphan hydrobromide; doxylamine succinate; acetaminophen products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Germany · Wick Medinait Mit Anisgeschmack
  • Spain · Ilvigrip Noche
  • Italy · Vicks Medinait

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/b29ad8b7-ddc5-4ce6-9360-77995c5ee00a
GET /v1/drugs/b29ad8b7-ddc5-4ce6-9360-77995c5ee00a?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; 3.125; 162.5",
  "substance": "DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; ACETAMINOPHEN",
  "productndc": "72854-085",
  "dosage_form": "TABLET, CHEWABLE",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1; mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about dextromethorphan hydrobromide; doxylamine succinate; 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.