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United States· US:58933-550_48824b85-d831-1ada-e063-6294a90a3793

Vicks DayQuil HOT REMEDY RAPID RELIEF MULTI-SYMPTOM

A medicinal product containing acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide, registered in United States by Procter & Gamble Manufactura S de RL de CV.

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 DayQuil HOT REMEDY RAPID RELIEF…ATC—REGISTER NO.US:58933-550_48824b85…PACKS LISTED4CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE
Manufacturer
Procter & Gamble Manufactura S de RL de CV
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
    58933-550-08
  • ndc11
    5893355001
    5 g in 1 PACKET (58933-550-01)
  • ndc11
    5893355008
    8 PACKET in 1 PACKAGE (58933-550-08) / 5 g in 1 PACKET
  • ndc11
    58933-550-01

Regulatory notes

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

Same medicine, other countries

Acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide in 2 other countries

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

All acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Czechia · Paralen Grip Chřipka A Kašel
  • Slovakia · Paralen Grip Chrípka A Kašeľ

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/6278f4ba-e612-4aa5-b7c3-3f331b7fb2d6
GET /v1/drugs/6278f4ba-e612-4aa5-b7c3-3f331b7fb2d6?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": "500; 10; 20",
  "substance": "ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE",
  "productndc": "58933-550",
  "dosage_form": "POWDER, FOR SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/5g; mg/5g; mg/5g",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide.

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.