United States· US:82160-238_2c493a3f-fb3a-99fc-e063-6394a90a76a8
Cornex
A medicinal product containing lactic acid; salicylic acid, registered in United States by Pella Pharmaceuticals 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
- LACTIC ACID; SALICYLIC ACID
- Manufacturer
- Pella Pharmaceuticals 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
- ndc1182160-238-01
- ndc1182160238011 TUBE in 1 CARTON (82160-238-01) / 15 g in 1 TUBE
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Lactic acid; salicylic acid in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomBazuka gelDiomed Developments Ltd
- GermanyClabin NPerrigo Deutschland Gmbh
- FranceDUOFILM, solution pour application cutanéeEG LABO - LABORATOIRES EUROGENERICS
- SpainANTIVERRUGAS ISDIN COLODIONIsdin S.A.
- IrelandSalactol CollodionDermal Laboratories (Ireland) Limited
- PolandAcerinAflofarm Farmacja Polska Sp. z o.o.
- SwedenVerruxin 200 mg/200 mg Kutan lösningKaro Pharma AS
- CzechiaDUOFILMSTADA Arzneimittel AG, Bad Vilbel
Authorised across Europe · EMA
The same active substance is authorised in 16 EEA countries. Names it is sold under:
- Austria · Duofilm, W-Tropfen
- Czechia · Duofilm
- Germany · Clabin N, Clabin Plus
- Estonia · Duofilm
- Spain · Antiverrugas, Verufil
- France · Duofilm, Kerafilm
- United Kingdom (Northern Ireland) · Bazuka, Bazuka Treatment
- Ireland · Salactol, Salatac
- Italy · Duofilm 16,7% + 15% Collodio, Verunec
- Latvia · Duofilm
- Netherlands · Duofilm
- Poland · Abe, Acerin
- Portugal · Calicida Indiano
- Romania · Duofilm
- Sweden · Verruxin
- Slovakia · Duofilm
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/bf765c75-f518-495d-bcdc-47e960c1c303 GET /v1/drugs/bf765c75-f518-495d-bcdc-47e960c1c303?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": "2505; 2505",
"substance": "LACTIC ACID; SALICYLIC ACID",
"productndc": "82160-238",
"dosage_form": "GEL",
"dea_schedule": null,
"strength_unit": "mg/15g; mg/15g",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER"
}See everything about lactic acid; salicylic acid.
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.