Back to search

United States· US:37662-0166_e3e1a345-0184-9cbe-e053-2a95a90adff0

Acidum Carbolicum

A medicinal product containing phenol, registered in United States by Hahnemann Laboratories, 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…normalisedAcidum CarbolicumATC—REGISTER NO.US:37662-0166_e3e1a34…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PHENOL
Manufacturer
Hahnemann Laboratories, 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 · 8

  • ndc11
    37662-0166-1
  • ndc11
    37662-0166-2
  • ndc11
    37662-0166-3
  • ndc11
    37662-0166-4
  • ndc11
    3766201661
    200 PELLET in 1 VIAL, GLASS (37662-0166-1)
  • ndc11
    3766201662
    500 PELLET in 1 VIAL, GLASS (37662-0166-2)
  • ndc11
    3766201663
    3000 PELLET in 1 BOTTLE, GLASS (37662-0166-3)
  • ndc11
    3766201664
    10000 PELLET in 1 BOTTLE, GLASS (37662-0166-4)

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Phenol in 5 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All phenol products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Germany · Bencard Negativ-Kontrolle, Pricktest Negativkontrolle
  • United Kingdom (Northern Ireland) · Oily Phenol Macarthys Laboratories
  • Italy · Fenolo Marco Viti

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/e6d45f3d-8f5a-4cbe-9510-6f7cf174715f
GET /v1/drugs/e6d45f3d-8f5a-4cbe-9510-6f7cf174715f?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": "1",
  "substance": "PHENOL",
  "productndc": "37662-0166",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "strength_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about phenol.

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.