63032-031 : Olux .5 mg/g Topical Aerosol, Foam


NDC: 63032-031
Labeler: Stiefel Laboratories Inc
Product Type: Human Prescription Drug
Drug Name:  Olux
Dosage Form: Topical Aerosol, Foam
Application #: NDA021142
Rev. Date: 


NDC Package Codes:

  • 63032-031-00: 100 G IN 1 CAN (63032‑031‑00)
  • 63032-031-50: 50 G IN 1 CAN (63032‑031‑50)

Active Ingredients:

  • Clobetasol Propionate

Dosage Strength:

  • .5 mg/g

Pharmaceutical Classes:

  • Corticosteroid [EPC]
  • Corticosteroid Hormone Receptor Agonists [MoA]

Related Products:

Based on records with the same trade name.
  • 0378-8182 Olux .5 mg/g Topical Aerosol, Foam by Mylan Pharmaceuticals Inc.
  • 40076-031 Olux .5 mg/g Topical Aerosol, Foam by Prestium Pharma, Inc.
  • 54868-5421 Olux .5 mg/g Topical Aerosol, Foam by Physicians Total Care, Inc.

NDC QR Code

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NDC 63032-031 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.