United States· US:72988-0033_ffc8ccb8-929d-8a6f-e053-6294a90ae29b

NOCOLD-S

A medicinal product containing chlorpheniramine maleate; acetaminophen, registered in United States by Lydia Co., Ltd..

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedNOCOLD-SATC—REGISTER NO.US:72988-0033_ffc8ccb…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CHLORPHENIRAMINE MALEATE; ACETAMINOPHEN
Manufacturer
Lydia Co., Ltd.
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
    7298800331
    20 mL in 1 BOTTLE (72988-0033-1)
  • ndc11
    72988-0033-1

Regulatory notes

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

Same medicine, other countries

Chlorpheniramine maleate; acetaminophen in 2 other countries

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

All chlorpheniramine maleate; acetaminophen products

Authorised across Europe · EMA

The same active substance is authorised in 9 EEA countries. Names it is sold under:

  • Belgium · Rhinofebryl
  • Bulgaria · Фервекс Настинка И Грип
  • France · Fervexrhume, Humexlib
  • Greece · Depon Cold & Flu
  • Italy · Baby Rinolo C.M., Efferalgan Influenza E Raffreddore
  • Luxembourg · Rhinofebryl
  • Poland · Fervex Extratabs
  • Portugal · Ben-U-Gripe, Cêgripe
  • Romania · Cemolplus, Fervex Răceală Și Gripă

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/b8e14967-ec54-435f-81f6-fe9eaf9c5cdc
GET /v1/drugs/b8e14967-ec54-435f-81f6-fe9eaf9c5cdc?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": "2.5; 200",
  "substance": "CHLORPHENIRAMINE MALEATE; ACETAMINOPHEN",
  "productndc": "72988-0033",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "mg/20mL; mg/20mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER"
}

See everything about chlorpheniramine maleate; 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.