United States· US:85593-102_3a5e2105-7126-183c-e063-6394a90ae879

SKIN TAG REMOVER

A medicinal product containing lactic acid; salicylic acid, registered in United States by Guangzhou ChuanMa International Trading 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…normalisedSKIN TAG REMOVERATC—REGISTER NO.US:85593-102_3a5e2105…PACKS LISTED2CHECKEDJune 26, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
LACTIC ACID; SALICYLIC ACID
Manufacturer
Guangzhou ChuanMa International Trading 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
June 26, 2026

Packs & prices · 2

  • ndc11
    8559310201
    20 mL in 1 BOTTLE (85593-102-01)
  • ndc11
    85593-102-01

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.

All lactic acid; salicylic acid products

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/dca782e1-404c-4d82-8f75-e6e1a26ec9cc
GET /v1/drugs/dca782e1-404c-4d82-8f75-e6e1a26ec9cc?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": "4.5; 15",
  "substance": "LACTIC ACID; SALICYLIC ACID",
  "productndc": "85593-102",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "strength_unit": "g/100mL; g/100mL",
  "application_number": "M028",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

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.