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United States· US:37000-518_4a172e6a-952f-dd6a-e063-6294a90a8484

Vicks NyQuil Severe

A medicinal product containing acetaminophen; dextromethorphan hydrobromide; doxylamine succinate; phenylephrine hydrochloride, 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 NyQuil SevereATC—REGISTER NO.US:37000-518_4a172e6a…PACKS LISTED6CHECKEDJune 26, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
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
June 26, 2026

Packs & prices · 6

  • ndc11
    37000-518-02
  • ndc11
    37000-518-08
  • ndc11
    37000-518-24
  • ndc11
    3700051802
    2 CAPSULE, LIQUID FILLED in 1 POUCH (37000-518-02)
  • ndc11
    3700051808
    1 BLISTER PACK in 1 CARTON (37000-518-08) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • ndc11
    3700051824
    2 BLISTER PACK in 1 CARTON (37000-518-24) / 12 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; phenylephrine hydrochloride in 1 other country

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

All acetaminophen; dextromethorphan hydrobromide; doxylamine succinate; phenylephrine hydrochloride products

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/ef7d1491-9a52-44a2-a860-3ba12dc28c9f
GET /v1/drugs/ef7d1491-9a52-44a2-a860-3ba12dc28c9f?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; 10; 6.25; 5",
  "substance": "ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE",
  "productndc": "37000-518",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1; mg/1; mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about acetaminophen; dextromethorphan hydrobromide; doxylamine succinate; phenylephrine hydrochloride.

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.