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United States· US:43689-0020_32934d7c-c3dc-4bfc-8b8c-ffbbc39768de

Earache Relief

A medicinal product containing atropa belladonna; oyster shell calcium carbonate, crude; matricaria chamomilla whole; calcium sulfide; potassium dichromate; lycopodium clavatum spore; plantago major whole; pulsatilla vulgaris whole, registered in United States by The Magni Company.

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…normalisedEarache ReliefATC—REGISTER NO.US:43689-0020_32934d7…PACKS LISTED2CHECKEDSeptember 27, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about atropa belladonna; oyster shell calcium carbonate, crude; matricaria chamomilla whole; calcium sulfide; potassium dichromate; lycopodium clavatum spore; plantago major whole; pulsatilla vulgaris wholeAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ATROPA BELLADONNA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; MATRICARIA CHAMOMILLA WHOLE; CALCIUM SULFIDE; POTASSIUM DICHROMATE; LYCOPODIUM CLAVATUM SPORE; PLANTAGO MAJOR WHOLE; PULSATILLA VULGARIS WHOLE
Manufacturer
The Magni Company
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
    4368900202
    1 BOTTLE in 1 PACKAGE (43689-0020-2) / 90 TABLET in 1 BOTTLE (43689-0020-1)
  • ndc11
    43689-0020-2

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/465915db-64f6-4252-a777-b263adc72755
GET /v1/drugs/465915db-64f6-4252-a777-b263adc72755?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": "12; 12; 12; 12; 12; 12; 12; 12",
  "substance": "ATROPA BELLADONNA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; MATRICARIA CHAMOMILLA WHOLE; CALCIUM SULFIDE; POTASSIUM DICHROMATE; LYCOPODIUM CLAVATUM SPORE; PLANTAGO MAJOR WHOLE; PULSATILLA VULGARIS WHOLE",
  "productndc": "43689-0020",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "strength_unit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}
API referenceMCP serverPlans

See everything about atropa belladonna; oyster shell calcium carbonate, crude; matricaria chamomilla whole; calcium sulfide; potassium dichromate; lycopodium clavatum spore; plantago major whole; pulsatilla vulgaris whole.

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.

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