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Drug company (FDA labeler)

Journey Medical Corporation

NDC labeler code: 69489

What is a labeler?

The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.

Official FDA data only

Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.

Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.

At a glance

8Products (NDC)

Prescription medicines

FDA applications for these products

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
ApprovedApplicationMedicineSponsor
November 1, 2024NDA219015 Minocycline hydrochloride
EMROSI
Journey
May 28, 2020NDA213690 Minocycline hydrochloride
ZILXI
Journey
October 18, 2019NDA212379 Minocycline hydrochloride
AMZEEQ
Journey
June 28, 2018NDA210361 Glycopyrronium
QBREXZA
Journey
February 28, 1989NDA018737 Sulconazole nitrate
EXELDERM
Journey
August 30, 1985NDA018738 Sulconazole nitrate
EXELDERM
Journey
November 8, 1982ANDA062269 Doxycycline
DOXYCYCLINE HYCLATE
Epic Pharma LLC
July 6, 1949NDA006927 Crotamiton
EURAX
Journey

The sponsor is the company that holds the FDA application; it can differ from the labeler.

Recall timeline

No recall of these products (by NDC code) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026

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