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United States· US:69423-968_50243df0-658e-67ff-e063-6294a90a3639

Vicks NyQuil Severe Honey

A medicinal product containing acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide; doxylamine succinate, registered in United States by 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 Severe HoneyATC—REGISTER NO.US:69423-968_50243df0…PACKS LISTED6CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
Manufacturer
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 · 6

  • ndc11
    69423-968-06
  • ndc11
    69423-968-08
  • ndc11
    6942396806
    177 mL in 1 BOTTLE, PLASTIC (69423-968-06)
  • ndc11
    6942396808
    236 mL in 1 BOTTLE, PLASTIC (69423-968-08)
  • ndc11
    6942396812
    354 mL in 1 BOTTLE, PLASTIC (69423-968-12)
  • ndc11
    69423-968-12

Regulatory notes

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

Same medicine, other countries

Acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide; doxylamine succinate in 1 other country

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

All acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide; doxylamine succinate 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/5f66990f-835f-4690-ad8d-9e6b06d97afe
GET /v1/drugs/5f66990f-835f-4690-ad8d-9e6b06d97afe?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; 5; 10; 6.25",
  "substance": "ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE",
  "productndc": "69423-968",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "mg/15mL; mg/15mL; mg/15mL; mg/15mL",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about acetaminophen; phenylephrine hydrochloride; 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.