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United States· US:85064-016_448e4aeb-09c9-2de6-e063-6294a90a96ba

EELHOE Probiotic Bright White Fresh

A medicinal product containing mentha piperita (peppermint) leaf, registered in United States by Shantou Eelhoe Daily Chemical Technology Co., Ltd..

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…normalisedEELHOE Probiotic Bright White FreshATC—REGISTER NO.US:85064-016_448e4aeb…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
MENTHA PIPERITA (PEPPERMINT) LEAF
Manufacturer
Shantou Eelhoe Daily Chemical Technology Co., Ltd.
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
    8506401601
    120 mg in 1 BOX (85064-016-01)
  • ndc11
    85064-016-01

Regulatory notes

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

Same medicine, other countries

Mentha piperita (peppermint) leaf in 3 other countries

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

All mentha piperita (peppermint) leaf products

Authorised across Europe · EMA

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

  • Austria · Dr. Kottas Pfefferminztee, Pfefferminztee Sidroga
  • Germany · Pfefferminzblätter Zum Trinken Nach Bereitung Eines Teeaufgusses|pflanzliches Magen-Darm-Mittel Aurica Naturheilmittel Und Naturwaren, Pfefferminzblätter Bombastus-Werke
  • Poland · Liść Mięty Pieprzowej, Mięta Fix

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/5cb35609-ab8c-4b34-a3db-110c920e2ccf
GET /v1/drugs/5cb35609-ab8c-4b34-a3db-110c920e2ccf?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": "TOPICAL",
  "source": "ndc",
  "strength": ".024",
  "substance": "MENTHA PIPERITA (PEPPERMINT) LEAF",
  "productndc": "85064-016",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "strength_unit": "mg/120mg",
  "application_number": "M022",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about mentha piperita (peppermint) leaf.

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.