United States· US:69729-133_575f6505-ff6d-5079-e063-6394a90accc2

COLDTAC ULTRA

A medicinal product containing phenylephrine hydrochloride; acetaminophen; chlorpheniramine maleate, registered in United States by OPMX LLC.

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedCOLDTAC ULTRAATC—REGISTER NO.US:69729-133_575f6505…PACKS LISTED5CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE
Manufacturer
OPMX LLC
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 · 5

  • ndc11
    69729-133-06
  • ndc11
    69729-133-27
  • ndc11
    69729-133-37
  • ndc11
    69729-133-38
  • ndc11
    69729-133-50

Regulatory notes

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

Same medicine, other countries

Phenylephrine hydrochloride; acetaminophen; chlorpheniramine maleate in 3 other countries

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

All phenylephrine hydrochloride; acetaminophen; chlorpheniramine maleate products

Authorised across Europe · EMA

The same active substance is authorised in 5 EEA countries. Names it is sold under:

  • Bulgaria · Тайлолфен Хот
  • Spain · Abacat, Anticatarral Edigen
  • Malta · Flucontrol Max
  • Poland · Flucontrol Hot, Flucontrol Max
  • Portugal · Gripalgin

Source: European Medicines Agency, Article 57 product data.

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/c80b5d0f-fdbe-4adc-a8ed-24fda9d3baf5
GET /v1/drugs/c80b5d0f-fdbe-4adc-a8ed-24fda9d3baf5?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; 500; 4",
  "substance": "PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE",
  "productndc": "69729-133",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "strength_unit": "mg/1; mg/1; mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about phenylephrine hydrochloride; acetaminophen; chlorpheniramine maleate.

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.