United States· US:85849-012_388f33c2-2be0-ded8-e063-6294a90aeeac
Plantar Fasciitis Cream
A medicinal product containing camphor, (-)-, registered in United States by SOLALIA LLC.
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
- CAMPHOR, (-)-
- Manufacturer
- SOLALIA LLC
- 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
- ndc11858490120150 mL in 1 CARTON (85849-012-01)
- ndc1185849-012-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Camphor, (-)- in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- PolandMaść kamforowaPoznańskie Zakłady Zielarskie "Herbapol" S.A.
- Japanｄ－カンフル
- FinlandCamphora EtnoviaEtnovia Oy
- GermanyMobil Schmerzfluid FranzbranntweinDr. Theiss Naturwaren Gmbh
- FranceCAMPHRICE DU CANADA 4 POUR CENT, bâton pour application localeLABORATOIRE DE L'HOMME DE FER
- BelgiumVicks VaporubP&G Health Belgium
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Bulgaria · Камфоров Спирт Химакс Фарма
- Germany · Mobil Schmerzfluid Franzbranntwein, Thüringer Franzbranntwein
- Estonia · Spiritus Camphoratus
- United Kingdom (Northern Ireland) · Soap Bpc Methylated
- Italy · Canfora Marco Viti, Canfora New.Fa.Dem.
- Poland · Camphorae Unguentum Farmina, Camphorae Unguentum Gemi
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/d08bb88d-b10c-48e5-ad44-b3761b535a00 GET /v1/drugs/d08bb88d-b10c-48e5-ad44-b3761b535a00?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": "50",
"substance": "CAMPHOR, (-)-",
"productndc": "85849-012",
"dosage_form": "CREAM",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about camphor, (-)-.
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.