United States· US:83818-015_383926b7-997c-af1e-e063-6394a90a506d
PHARMBANNER Anti-Fungal Shampoo.
A medicinal product containing hexamidine diisethionate, registered in United States by Shenzhen Xinxin Yunhai Technology Co., Ltd..
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- HEXAMIDINE DIISETHIONATE
- Manufacturer
- Shenzhen Xinxin Yunhai Technology 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
- ndc118381801501250 mL in 1 BOTTLE (83818-015-01)
- ndc1183818-015-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Hexamidine diisethionate in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumDesomedine 0.1 %Bausch & Lomb Pharma
- CzechiaZAMISEPTLaboratoires Thea, Clermont-Ferrand
- GermanyLaryngomedin NCassella-Med Gmbh & Co. Kg
- FinlandZamiseptLaboratoires Thea
- FranceZAMELINE 1 mg/mL, collyre en solutionTHEA
- SwedenZamisept 1 mg/ml Ögondroppar, lösningLaboratoires THEA
Authorised across Europe · EMA
The same active substance is authorised in 17 EEA countries. Names it is sold under:
- Belgium · Desomedine, Hexomedine Lösung
- Bulgaria · Замидин
- Czechia · Zamisept
- Germany · Laryngomedin N, Zamidine
- Denmark · Zamisept
- Finland · Zamisept
- France · Desomedine, Hexamidine Gilbert
- Greece · Zameline
- Iceland · Zameline
- Italy · Zamidine
- Luxembourg · Desomedine, Hexomedine Lösung
- Norway · Zamisept
- Poland · Zamidine
- Portugal · Zamisept
- Romania · Zamidine
- Sweden · Zamisept
- Slovakia · Zamisept
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/1678994a-9126-4177-ae2f-e56272612ee7 GET /v1/drugs/1678994a-9126-4177-ae2f-e56272612ee7?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": ".1",
"substance": "HEXAMIDINE DIISETHIONATE",
"productndc": "83818-015",
"dosage_form": "SHAMPOO",
"dea_schedule": null,
"strength_unit": "g/100mL",
"application_number": "M032",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about hexamidine diisethionate.
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.