United States· US:69423-804_42f17c7f-5909-c556-e063-6294a90a148e

Vicks NyQuil

A medicinal product containing doxylamine succinate; dextromethorphan hydrobromide; acetaminophen, registered in United States by The Procter & Gamble Manufacturing Company.

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…normalisedVicks NyQuilATC—REGISTER NO.US:69423-804_42f17c7f…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DOXYLAMINE SUCCINATE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN
Manufacturer
The Procter & Gamble Manufacturing Company
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
    6942380424
    1 BOTTLE in 1 CARTON (69423-804-24) / 24 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • ndc11
    69423-804-24

Regulatory notes

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

Same medicine, other countries

Doxylamine succinate; dextromethorphan hydrobromide; acetaminophen in 3 other countries

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

All doxylamine succinate; dextromethorphan hydrobromide; 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/f9a41611-8f3f-41a1-8d5d-9a8e17bcf80c
GET /v1/drugs/f9a41611-8f3f-41a1-8d5d-9a8e17bcf80c?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": "6.25; 10; 325",
  "substance": "DOXYLAMINE SUCCINATE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN",
  "productndc": "69423-804",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1; mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about doxylamine succinate; 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.