NDC 72934-4748

MINOXIDIL 7% / PROGESTERONE 0.1%

Minoxidil 7% / Progesterone 0.1%

MINOXIDIL 7% / PROGESTERONE 0.1% is a Topical Solution in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Minoxidil; Progesterone.

Product ID72934-4748_8747e14a-9839-bdcc-e053-2995a90adc35
NDC72934-4748
Product TypeHuman Prescription Drug
Proprietary NameMINOXIDIL 7% / PROGESTERONE 0.1%
Generic NameMinoxidil 7% / Progesterone 0.1%
Dosage FormSolution
Route of AdministrationTOPICAL
Marketing Start Date2019-05-01
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameSincerus Florida, LLC
Substance NameMINOXIDIL; PROGESTERONE
Active Ingredient Strength7 g/100g; g/100g
Pharm ClassesArteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC],Progesterone [CS],Progesterone [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 72934-4748-8

60 g in 1 BOTTLE, GLASS (72934-4748-8)
Marketing Start Date2019-05-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72934-4748-8 [72934474808]

MINOXIDIL 7% / PROGESTERONE 0.1% SOLUTION
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2019-05-01

Drug Details

Active Ingredients

IngredientStrength
MINOXIDIL7 g/100g

Pharmacological Class

  • Arteriolar Vasodilation [PE]
  • Arteriolar Vasodilator [EPC]
  • Progesterone [CS]
  • Progesterone [EPC]
  • Arteriolar Vasodilation [PE]
  • Arteriolar Vasodilator [EPC]
  • Progesterone [CS]
  • Progesterone [EPC]

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