72934-4080 : Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1% Topical Solution


NDC: 72934-4080
Labeler: Sincerus Florida, LLC
Product Type: Human Prescription Drug
Drug Name: Fluocinolone Acetonide 0.01% / Minoxidil 7% / Progesterone 0.1%
Dosage Form: Topical Solution
Rev. Date: 


NDC Package Codes:

  • 72934-4080-8: 60 G IN 1 BOTTLE, GLASS (72934‑4080‑8)

Active Ingredients:

  • Fluocinolone Acetonide
  • Minoxidil
  • Progesterone

Dosage Strength:

  • .01 g/100g
  • 7 g/100g
  • .1 g/100g

Pharmaceutical Classes:

  • Corticosteroid [EPC]
  • Corticosteroid Hormone Receptor Agonists [MoA]
  • Arteriolar Vasodilation [PE]
  • Arteriolar Vasodilator [EPC]
  • Progesterone [CS]
  • Progesterone [EPC]

NDC QR Code

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NDC 72934-4080 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.