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United States· US:47682-835_3e4fe7f8-b07f-5ac2-e063-6394a90afc08

Medi-First Cough Cold

A medicinal product containing phenylephrine hydrochloride; acetaminophen; dextromethorphan hydrobromide; guaifenesin, 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…normalisedMedi-First Cough ColdATC—REGISTER NO.US:47682-835_3e4fe7f8…PACKS LISTED6CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
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
    4768283536
    75 PACKET in 1 BOX (47682-835-36) / 2 TABLET, FILM COATED in 1 PACKET (47682-835-99)
  • ndc11
    4768283580
    40 PACKET in 1 BOX (47682-835-80) / 2 TABLET, FILM COATED in 1 PACKET (47682-835-99)
  • ndc11
    4768283599
    2 TABLET, FILM COATED in 1 PACKET (47682-835-99)
  • ndc11
    47682-835-36
  • ndc11
    47682-835-80
  • ndc11
    47682-835-99

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.

All phenylephrine hydrochloride; acetaminophen; dextromethorphan hydrobromide; guaifenesin 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/6fc3ef02-b08e-448f-99d4-ae45e64fa8bd
GET /v1/drugs/6fc3ef02-b08e-448f-99d4-ae45e64fa8bd?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; 100",
  "substance": "PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
  "productndc": "47682-835",
  "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 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.