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United States· US:0363-8996_48c201e3-e57a-f0c2-e063-6294a90a95ca

SEVERE DAYTIME COLD and FLU

A medicinal product containing guaifenesin; dextromethorphan hydrobromide; phenylephrine hydrochloride; acetaminophen, registered in United States by Walgreens.

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…normalisedSEVERE DAYTIME COLD and FLUATC—REGISTER NO.US:0363-8996_48c201e3…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN
Manufacturer
Walgreens
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 · 2

  • ndc11
    0363899624
    2 BLISTER PACK in 1 CARTON (0363-8996-24) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • ndc11
    0363-8996-24

Regulatory notes

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

Same medicine, other countries

Guaifenesin; dextromethorphan hydrobromide; phenylephrine hydrochloride; acetaminophen in 1 other country

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

All guaifenesin; dextromethorphan hydrobromide; phenylephrine hydrochloride; acetaminophen 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/e821fab9-85d6-497d-8344-5982f34f984b
GET /v1/drugs/e821fab9-85d6-497d-8344-5982f34f984b?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": "200; 10; 5; 325",
  "substance": "GUAIFENESIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN",
  "productndc": "0363-8996",
  "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 guaifenesin; dextromethorphan hydrobromide; phenylephrine hydrochloride; acetaminophen.

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.