United States· US:43857-0645_f7bbfab2-45d8-4e99-9d42-685a6d15050f
Epiforce P
A medicinal product, registered in United States by BioActive Nutritional, 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)- Manufacturer
- BioActive Nutritional, 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 · 2
- ndc11438570645130 mL in 1 BOTTLE, DROPPER (43857-0645-1)
- ndc1143857-0645-1
Regulatory notes
No shortage, Orange Book or US label notes for this record.
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/d96ce3e4-bd57-46cf-90a6-bbf1c31b6ae8 GET /v1/drugs/d96ce3e4-bd57-46cf-90a6-bbf1c31b6ae8?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": "3; 3; 3; 3; 3; 3; 3; 3; 3; 4; 5; 12; 12; 12; 12; 12; 12; 12; 12; 12",
"substance": "BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; ECHINACEA ANGUSTIFOLIA WHOLE; GLYCYRRHIZA GLABRA; ARCTIUM LAPPA ROOT; FRANGULA ALNUS BARK; FRANGULA PURSHIANA BARK; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARK; PHYTOLACCA AMERICANA ROOT; GOLDENSEAL; ARSENIC TRIIODIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CLEMATIS RECTA FLOWERING TOP; GRAPHITE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; DAPHNE MEZEREUM BARK; KEROSENE; SEPIA OFFICINALIS JUICE",
"productndc": "43857-0645",
"dosage_form": "LIQUID",
"dea_schedule": null,
"strength_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_Q]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about Epiforce.
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.