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United States· US:47682-047_3e4c8eb0-708e-774b-e063-6294a90a8436

Multi-Symptom Cold Relief

A medicinal product containing dextromethorphan hydrobromide; guaifenesin; acetaminophen; phenylephrine hydrochloride, registered in United States by Unifirst First Aid Corporation.

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…normalisedMulti-Symptom Cold ReliefATC—REGISTER NO.US:47682-047_3e4c8eb0…PACKS LISTED6CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Manufacturer
Unifirst First Aid Corporation
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 · 6

  • ndc11
    4768204747
    100 PACKET in 1 BOX (47682-047-47) / 2 TABLET, FILM COATED in 1 PACKET (47682-047-99)
  • ndc11
    4768204780
    40 PACKET in 1 BOX (47682-047-80) / 2 TABLET, FILM COATED in 1 PACKET (47682-047-99)
  • ndc11
    4768204799
    2 TABLET, FILM COATED in 1 PACKET (47682-047-99)
  • ndc11
    47682-047-80
  • ndc11
    47682-047-99
  • ndc11
    47682-047-47

Regulatory notes

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

Same medicine, other countries

Dextromethorphan hydrobromide; guaifenesin; acetaminophen; phenylephrine hydrochloride 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; acetaminophen; phenylephrine hydrochloride 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/c3eb3265-92fe-42de-a6b4-e93222aebb22
GET /v1/drugs/c3eb3265-92fe-42de-a6b4-e93222aebb22?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; 100; 325; 5",
  "substance": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE",
  "productndc": "47682-047",
  "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; acetaminophen; phenylephrine hydrochloride.

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.