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United States· US:84167-192_58860bba-91eb-c63f-e063-6394a90ac91c

APUREE Prorevive Maximum Strength Antifungal

A medicinal product containing undecylenic acid; zinc undecylenate, registered in United States by Guangzhou Meixi Biotechnology 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…normalisedAPUREE Prorevive Maximum Strength Ant…ATC—REGISTER NO.US:84167-192_58860bba…PACKS LISTED1CHECKEDSeptember 27, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about undecylenic acid; zinc undecylenateAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
UNDECYLENIC ACID; ZINC UNDECYLENATE
Manufacturer
Guangzhou Meixi Biotechnology 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 · 1

  • ndc11
    84167-192-11

Regulatory notes

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

Same medicine, other countries

Undecylenic acid; zinc undecylenate in 3 other countries

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

All undecylenic acid; zinc undecylenate products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • United Kingdom (Northern Ireland) · Mycota
  • Ireland · Desenex
  • Poland · Ungentum Undecylenicum

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/2737c208-5887-406f-8763-da946669c637
GET /v1/drugs/2737c208-5887-406f-8763-da946669c637?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": "TOPICAL",
  "source": "ndc",
  "strength": "15; 10",
  "substance": "UNDECYLENIC ACID; ZINC UNDECYLENATE",
  "productndc": "84167-192",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "strength_unit": "g/1; g/1",
  "application_number": "M006",
  "marketing_category": "OTC MONOGRAPH DRUG"
}
API referenceMCP serverPlans

See everything about undecylenic acid; zinc undecylenate.

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.

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