United States· US:66096-115_d44af2b7-f773-3d27-e053-2a95a90abc46

Cough Relief

A medicinal product containing aconitum napellus; antimony trisulfide; antimony pentasulfide; antimony potassium tartrate; aralia racemosa root; bryonia alba root; chelidonium majus; copper; drosera rotundifolia; calcium sulfide; potassium carbonate; spongia officinalis skeleton, roasted, registered in United States by OHM PHARMA 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…normalisedCough ReliefATC—REGISTER NO.US:66096-115_d44af2b7…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ACONITUM NAPELLUS; ANTIMONY TRISULFIDE; ANTIMONY PENTASULFIDE; ANTIMONY POTASSIUM TARTRATE; ARALIA RACEMOSA ROOT; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS; COPPER; DROSERA ROTUNDIFOLIA; CALCIUM SULFIDE; POTASSIUM CARBONATE; SPONGIA OFFICINALIS SKELETON, ROASTED
Manufacturer
OHM PHARMA 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
    6609611505
    59 mL in 1 BOTTLE, SPRAY (66096-115-05)
  • ndc11
    66096-115-05

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/0519a0b2-5e74-4723-bff1-dbb93296280b
GET /v1/drugs/0519a0b2-5e74-4723-bff1-dbb93296280b?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": "6; 8; 8; 8; 4; 6; 6; 12; 6; 12; 12; 6",
  "substance": "ACONITUM NAPELLUS; ANTIMONY TRISULFIDE; ANTIMONY PENTASULFIDE; ANTIMONY POTASSIUM TARTRATE; ARALIA RACEMOSA ROOT; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS; COPPER; DROSERA ROTUNDIFOLIA; CALCIUM SULFIDE; POTASSIUM CARBONATE; SPONGIA OFFICINALIS SKELETON, ROASTED",
  "productndc": "66096-115",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about aconitum napellus; antimony trisulfide; antimony pentasulfide; antimony potassium tartrate; aralia racemosa root; bryonia alba root; chelidonium majus; copper; drosera rotundifolia; calcium sulfide; potassium carbonate; spongia officinalis skeleton, roasted.

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.