United States· US:63868-140_7a62eb8f-1148-4dba-845b-d5c67ea7d033

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…normalisedCold and FluATC—REGISTER NO.US:63868-140_7a62eb8f…PACKS LISTED4CHECKEDSeptember 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 · 4

  • ndc11
    63868-140-08
  • ndc11
    63868-140-12
  • ndc11
    6386814008
    237 mL in 1 BOTTLE, PLASTIC (63868-140-08)
  • ndc11
    6386814012
    355 mL in 1 BOTTLE, PLASTIC (63868-140-12)

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/c3c234aa-02a8-48e8-805f-c917af19c4d0
GET /v1/drugs/c3c234aa-02a8-48e8-805f-c917af19c4d0?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": "650; 30; 12.5",
  "substance": "ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE",
  "productndc": "63868-140",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "mg/30mL; mg/30mL; mg/30mL",
  "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.