United States· US:37000-517_4a1728b9-82b0-bafa-e063-6294a90a1fca
Vicks DayQuil Severe
A medicinal product containing phenylephrine hydrochloride; acetaminophen; dextromethorphan hydrobromide; guaifenesin, registered in United States by The Procter & Gamble Manufacturing Company.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- 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
- September 27, 2026
Packs & prices · 8
- ndc1137000-517-02
- ndc1137000-517-08
- ndc1137000-517-16
- ndc1137000-517-24
- ndc1137000517022 CAPSULE, LIQUID FILLED in 1 POUCH (37000-517-02)
- ndc1137000517081 BLISTER PACK in 1 CARTON (37000-517-08) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
- ndc1137000517162 BLISTER PACK in 1 CARTON (37000-517-16) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
- ndc1137000517242 BLISTER PACK in 1 CARTON (37000-517-24) / 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
Phenylephrine hydrochloride; acetaminophen; dextromethorphan hydrobromide; guaifenesin in 1 other country
What each register calls a product with the same active substance — salts and hydrates count as the same.
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/3374a520-8e25-42c9-a1d3-8b7ea0e32a9b GET /v1/drugs/3374a520-8e25-42c9-a1d3-8b7ea0e32a9b?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": "5; 325; 10; 200",
"substance": "PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"productndc": "37000-517",
"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 phenylephrine hydrochloride; acetaminophen; dextromethorphan hydrobromide; guaifenesin.
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.