United States· US:58264-0163_2b9f0ae7-5ebc-31e5-e063-6294a90a6ebf

D-139

A medicinal product containing anemone pratensis; lycopodium clavatum spore; phosphorus; ferrosoferric phosphate; arsenic triiodide; atropa belladonna; sodium phosphate, dibasic, heptahydrate; activated charcoal; oyster shell calcium carbonate, crude; goldenseal; strychnos nux-vomica seed, registered in United States by DNA Labs, Inc..

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedD-139ATC—REGISTER NO.US:58264-0163_2b9f0ae…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ANEMONE PRATENSIS; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; FERROSOFERRIC PHOSPHATE; ARSENIC TRIIODIDE; ATROPA BELLADONNA; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; ACTIVATED CHARCOAL; OYSTER SHELL CALCIUM CARBONATE, CRUDE; GOLDENSEAL; STRYCHNOS NUX-VOMICA SEED
Manufacturer
DNA Labs, 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

  • ndc11
    5826401631
    29.57 mL in 1 BOTTLE, GLASS (58264-0163-1)
  • ndc11
    58264-0163-1

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/24435ff8-6dbe-4cf2-b1e0-2d08788ad6cc
GET /v1/drugs/24435ff8-6dbe-4cf2-b1e0-2d08788ad6cc?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": "SUBLINGUAL",
  "source": "ndc",
  "strength": "6; 6; 6; 6; 6; 6; 6; 6; 6; 3; 6",
  "substance": "ANEMONE PRATENSIS; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; FERROSOFERRIC PHOSPHATE; ARSENIC TRIIODIDE; ATROPA BELLADONNA; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; ACTIVATED CHARCOAL; OYSTER SHELL CALCIUM CARBONATE, CRUDE; GOLDENSEAL; STRYCHNOS NUX-VOMICA SEED",
  "productndc": "58264-0163",
  "dosage_form": "SOLUTION",
  "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_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about anemone pratensis; lycopodium clavatum spore; phosphorus; ferrosoferric phosphate; arsenic triiodide; atropa belladonna; sodium phosphate, dibasic, heptahydrate; activated charcoal; oyster shell calcium carbonate, crude; goldenseal; strychnos nux-vomica seed.

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.