United States· US:37662-2090_efcdc393-5dac-38d1-e053-2995a90acb2e
Silicea
A medicinal product containing silicon dioxide, 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
- SILICON DIOXIDE
- 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
- ndc11376622090180 PELLET in 1 VIAL, GLASS (37662-2090-1)
- ndc113766220902200 PELLET in 1 VIAL, GLASS (37662-2090-2)
- ndc1137662209031200 PELLET in 1 BOTTLE, GLASS (37662-2090-3)
- ndc1137662209044000 PELLET in 1 BOTTLE, GLASS (37662-2090-4)
- ndc1137662-2090-4
- ndc1137662-2090-1
- ndc1137662-2090-2
- ndc1137662-2090-3
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Silicon dioxide in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumSilicea Boiron 12CHBoiron
- NetherlandsSiliceaHeel Belgium n.v.
- SwitzerlandHübner Silicea Balsam, Gel zum EinnehmenDermapharm AG
- GermanyKieselerde Salus PharmaSalus Pharma Gmbh
- FinlandQuarz Weleda
- FranceSILICEA NATURALE (QUARTZ) WELEDA, degré de dilution compris entre 2CH et 30CH ou entre 4DH et 60DHWELEDA
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- Germany · Kieselerde Salus Pharma, Kieselerde Zur Anwendung Bei Erwachsenen Und Jugendlichen Ab 12 Jahren I.B. Pharma-Vertriebs
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/aa7596f1-5c4b-4a34-9160-e4c8146b8824 GET /v1/drugs/aa7596f1-5c4b-4a34-9160-e4c8146b8824?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": "30",
"substance": "SILICON DIOXIDE",
"productndc": "37662-2090",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about silicon dioxide.
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.