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United States· US:63868-737_aa1e6dc2-aea5-48d9-8f59-d13a3075f6d8

Night Time Cold and Flu

A medicinal product containing acetaminophen; dextromethorphan hydrobromide; doxylamine succinate, registered in United States by QUALITY CHOICE (Chain Drug Marketing Association).

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…normalisedNight Time Cold and FluATC—REGISTER NO.US:63868-737_aa1e6dc2…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
Manufacturer
QUALITY CHOICE (Chain Drug Marketing Association)
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
    63868-737-24
  • ndc11
    6386873724
    24 BLISTER PACK in 1 CARTON (63868-737-24) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Regulatory notes

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

Same medicine, other countries

Acetaminophen; dextromethorphan hydrobromide; doxylamine succinate in 3 other countries

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

All acetaminophen; dextromethorphan hydrobromide; doxylamine succinate 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/e5e2d479-99f8-4383-88d4-b2f72084016c
GET /v1/drugs/e5e2d479-99f8-4383-88d4-b2f72084016c?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": "325; 15; 6.25",
  "substance": "ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE",
  "productndc": "63868-737",
  "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 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.