Dermatitis

• FDA label_change · 2026-03-16
  FDA Approved: DESOXIMETASONE — Supplemental Application (Saptalis Pharmaceuticals, LLC.)

  FDA approved a supplemental application for desoximetasone (Saptalis Pharmaceuticals, LLC.), resulting in updated labeling for this topical …

• FDA label_change · 2024-06-11
  FDA Approved: HYDROCORTISONE — Supplemental Application (Aurobindo Pharma Limited)

  FDA approved a Supplemental Application for HYDROCORTISONE from Aurobindo Pharma Limited, typically indicating a label change for this gener…

• FDA label_change · 2023-07-17
  FDA Approved: BETAMETHASONE DIPROPIONATE — Supplemental Application (Viona Pharmaceuticals Inc)

  The FDA approved a supplemental application for Betamethasone Dipropionate from Viona Pharmaceuticals Inc, typically reflecting labeling cha…

• FDA label_change · 2017-01-13
  FDA Approved: CORDRAN — Supplemental Application (Almirall, LLC)

  FDA approved a supplemental application for CORDRAN (flurandrenolide) filed by Almirall, LLC, likely affecting labeling.

• FDA label_change · 2015-06-29
  FDA Approved: CLOBETASOL PROPIONATE — Supplemental Application (Actavis Pharma, Inc.)

  FDA approves a supplemental application for clobetasol propionate from Actavis Pharma, Inc. to update the product labeling.

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• FDA label_change · 2015-05-21
  FDA Approved: CLOBEX — Supplemental Application (Galderma Laboratories, L.P.)

  The FDA approved a supplemental application for CLOBEX (clobetasol propionate) from Galderma Laboratories to update the product labeling.

• FDA label_change · 2014-10-30
  FDA Approved: HYDROCORTISONE BUTYRATE — Supplemental Application (Oceanside Pharmaceuticals)

  FDA approved a supplemental application for hydrocortisone butyrate from Oceanside Pharmaceuticals, resulting in changes to the product labe…

• FDA label_change · 2014-04-02
  FDA Approved: HALOG — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

  FDA supplemental application for HALOG (halcinonide cream) submitted by Sun Pharmaceutical Industries, Inc., with the submission status indi…

• FDA label_change · 2007-12-12
  FDA Approved: DERMOTIC — Supplemental Application (Royal Pharmaceuticals)

  FDA approved a supplemental application for DERMOTIC (fluocinonide acetate) submitted by Royal Pharmaceuticals, typically resulting in updat…