United States· US:63545-900_2b4a9c74-d8fd-54ab-e063-6294a90a6799
Aluminium sulphuricum
A medicinal product containing aluminum sulfate, registered in United States by Hahnemann Laboratories, Inc..
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
- ALUMINUM SULFATE
- Manufacturer
- Hahnemann Laboratories, Inc.
- 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 · 8
- ndc1163545-900-04
- ndc1163545-900-01
- ndc1163545-900-02
- ndc1163545-900-03
- ndc116354590001200 PELLET in 1 VIAL, GLASS (63545-900-01)
- ndc116354590002500 PELLET in 1 VIAL, GLASS (63545-900-02)
- ndc1163545900033000 PELLET in 1 BOTTLE, GLASS (63545-900-03)
- ndc11635459000410000 PELLET in 1 BOTTLE, GLASS (63545-900-04)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Aluminum sulfate in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomActonorm gelWallace Manufacturing Chemists Ltd
- BelgiumAlumina Boiron 15CHBoiron
- FinlandAlumina
- NetherlandsAluminaHeel Belgium n.v.
- PolandAntidralTeva Pharmaceuticals Polska Sp. z o.o.
- GermanyGargarisma Zum GurgelnHermes Arzneimittel Gmbh
- IrelandAnhydrol Forte 20% w/v Cutaneous SolutionDermal Laboratories (Ireland) Limited
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Germany · Gargarisma Zum Gurgeln, Mallebrin
- United Kingdom (Northern Ireland) · Anhydrol Forte
- Hungary · Solutio Antisudorica Fono Viii.
- Ireland · Anhydrol Forte
- Poland · Antidral, Gelatum Aluminii Phosphorici Pf Ziololek
- Portugal · Almigástrico, Pepsamar
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/0e93b6ef-8cce-48d9-9a63-2b29ab683ea5 GET /v1/drugs/0e93b6ef-8cce-48d9-9a63-2b29ab683ea5?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": "100",
"substance": "ALUMINUM SULFATE",
"productndc": "63545-900",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about aluminum sulfate.
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.