United States· US:87762-001_539567e0-2d0d-c001-e063-6294a90a4683
Nano Eye Drop Serum
A medicinal product containing mentha piperita leaf, registered in United States by Shenzhen Yiyang Zhiting Technology Co., Ltd.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- MENTHA PIPERITA LEAF
- Manufacturer
- Shenzhen Yiyang Zhiting 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 · 1
- ndc1187762-001-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Mentha piperita leaf in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- GermanyPfefferminzblätter Zum Trinken Nach Bereitung Eines Teeaufgusses|pflanzliches Magen-Darm-Mittel Aurica Naturheilmittel Und NaturwarenAurica Naturheilmittel Und Naturwaren Gmbh
- PolandLiść Mięty pieprzowejKrakowskie Zakłady Zielarskie "Herbapol" w Krakowie S.A.
- SwitzerlandSidroga Pfefferminzblätter, ArzneiteeUriach Switzerland AG
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/f2f19ee6-2305-43a5-9df8-9e8c743c431a GET /v1/drugs/f2f19ee6-2305-43a5-9df8-9e8c743c431a?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": "1",
"substance": "MENTHA PIPERITA LEAF",
"productndc": "87762-001",
"dosage_form": "LIQUID",
"dea_schedule": null,
"strength_unit": "mg/3000mg",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about mentha piperita 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.