Back to search

United States· US:85817-006_413e76b5-263d-62fa-e063-6294a90a9214

Arflom Toenail Fungus Treatment Liquid

A undecylenic acid product containing undecylenic acid, registered in United States by Guangzhou Qiexiran Cosmetics Co., Ltd.. The same ATC class is registered in 4 of our 19 countries.

ATC D01AE04US 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…normalisedArflom Toenail Fungus Treatment LiquidATCD01AE04REGISTER NO.US:85817-006_413e76b5…PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Undecylenic acid is registered in 4 of 19 countries.

Countries holding a registration under ATC D01AE04 (undecylenic acid), each read from that country’s own register.

  • This record: United States, from FDA National Drug Code directory (United States)
  • 3 of them publish a price we can compare per daily dose

Undecylenic acid · ATC D01AE04

4 / 19 countries

  • Ireland
  • Polandprice
  • Switzerlandprice
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
UNDECYLENIC ACID
Manufacturer
Guangzhou Qiexiran Cosmetics Co., Ltd.
Country
United States (US)
ATC code
D01AE04
ATC class
Undecylenic acid
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    85817-006-01
  • ndc11
    8581700601
    2 BOTTLE in 1 BOX (85817-006-01) / 15 mL in 1 BOTTLE

Regulatory notes

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

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/90438893-7c35-4752-b88f-eefb77555740
GET /v1/drugs/90438893-7c35-4752-b88f-eefb77555740?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": "25",
  "substance": "UNDECYLENIC ACID",
  "productndc": "85817-006",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "g/100mL",
  "application_number": "M005",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about undecylenic acid.

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.