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United States· US:41226-675_35c8c6ce-c850-6d95-e063-6294a90afe26

Daytime Cold and Flu

A medicinal product containing dextromethorphan hydrobromide; guaifenesin; phenylephrine hydrochloride; acetaminophen, registered in United States by KROGER 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…normalisedDaytime Cold and FluATC—REGISTER NO.US:41226-675_35c8c6ce…PACKS LISTED2CHECKEDSeptember 6, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN
Manufacturer
KROGER 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 6, 2026

Packs & prices · 2

  • ndc11
    4122667524
    2 BLISTER PACK in 1 CARTON (41226-675-24) / 12 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    41226-675-24

Regulatory notes

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

Same medicine, other countries

Dextromethorphan hydrobromide; guaifenesin; 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 dextromethorphan hydrobromide; guaifenesin; 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/de0b9d79-5b04-48b9-8d45-1577dc9e0439
GET /v1/drugs/de0b9d79-5b04-48b9-8d45-1577dc9e0439?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": "10; 200; 5; 325",
  "substance": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN",
  "productndc": "41226-675",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1; mg/1; mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about dextromethorphan hydrobromide; guaifenesin; 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.