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United States· US:84735-006_35a13839-b5ed-19ab-e063-6294a90a7115

MILIA REMOVER TREATMENT

A medicinal product containing didecyldimonium, registered in United States by Hengyang Chuangjiujia Trading Co., Ltd..

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…normalisedMILIA REMOVER TREATMENTATC—REGISTER NO.US:84735-006_35a13839…PACKS LISTED2CHECKEDJuly 26, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DIDECYLDIMONIUM
Manufacturer
Hengyang Chuangjiujia Trading 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
July 26, 2026

Packs & prices · 2

  • ndc11
    84735-006-01
  • ndc11
    8473500601
    1 BOTTLE in 1 BOX (84735-006-01) / 30 mL in 1 BOTTLE

Regulatory notes

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

Same medicine, other countries

Didecyldimonium in 3 other countries

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

All didecyldimonium products

Authorised across Europe · EMA

The same active substance is authorised in 1 EEA country. Names it is sold under:

  • Germany · Amosept

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/ac511ce8-6b3d-4deb-bed2-71f690b4e8aa
GET /v1/drugs/ac511ce8-6b3d-4deb-bed2-71f690b4e8aa?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": ".025",
  "substance": "DIDECYLDIMONIUM",
  "productndc": "84735-006",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "g/100mL",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about didecyldimonium.

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.