United States· US:69423-806_44700b29-ff75-d10d-e063-6294a90a1a04
VICKS DayQuil SEVERE HONEY FLAVOR
A medicinal product containing acetaminophen; phenylephrine hydrochloride; dextromethorphan hydrobromide; guaifenesin, registered in United States by 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
- ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- 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 · 4
- ndc116942380608236 mL in 1 BOTTLE, PLASTIC (69423-806-08)
- ndc116942380612354 mL in 1 BOTTLE, PLASTIC (69423-806-12)
- ndc1169423-806-08
- ndc1169423-806-12
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Acetaminophen; phenylephrine hydrochloride; 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/4ad18c56-0565-4b27-9f9c-863cdd8832fa GET /v1/drugs/4ad18c56-0565-4b27-9f9c-863cdd8832fa?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; 200",
"substance": "ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"productndc": "69423-806",
"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; 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.