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United States· US:84983-031_508190ae-6314-b522-e063-6394a90a9c38

Mouth Relief Liquid

A medicinal product containing mentha piperita (peppermint) leaf, registered in United States by Shantou South Moon Biotechnology 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…normalisedMouth Relief LiquidATC—REGISTER NO.US:84983-031_508190ae…PACKS LISTED2CHECKEDJuly 26, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about mentha piperita (peppermint) leafAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
MENTHA PIPERITA (PEPPERMINT) LEAF
Manufacturer
Shantou South Moon Biotechnology 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
July 26, 2026

Packs & prices · 2

  • ndc11
    84983-031-01
  • ndc11
    8498303101
    25 mg in 1 BOTTLE, PLASTIC (84983-031-01)

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/dda42b4f-eb14-4099-add0-dbfa78625590
GET /v1/drugs/dda42b4f-eb14-4099-add0-dbfa78625590?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": ".075",
  "substance": "MENTHA PIPERITA (PEPPERMINT) LEAF",
  "productndc": "84983-031",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "mg/25mg",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG"
}
API referenceMCP serverPlans

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.

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