NDC 72934-4150

MINOXIDIL 7% / TRETINOIN 0.025%

Minoxidil 7% / Tretinoin 0.025%

MINOXIDIL 7% / TRETINOIN 0.025% is a Topical Solution in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Tretinoin; Minoxidil.

Product ID72934-4150_883c10fa-cb98-4879-e053-2a95a90aabb5
NDC72934-4150
Product TypeHuman Prescription Drug
Proprietary NameMINOXIDIL 7% / TRETINOIN 0.025%
Generic NameMinoxidil 7% / Tretinoin 0.025%
Dosage FormSolution
Route of AdministrationTOPICAL
Marketing Start Date2019-05-07
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameSincerus Florida, LLC
Substance NameTRETINOIN; MINOXIDIL
Active Ingredient Strength0 g/100g; g/100g
Pharm ClassesRetinoid [EPC],Retinoids [CS],Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 72934-4150-8

60 g in 1 BOTTLE, GLASS (72934-4150-8)
Marketing Start Date2019-05-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72934-4150-8 [72934415008]

MINOXIDIL 7% / TRETINOIN 0.025% SOLUTION
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-07

Drug Details

Active Ingredients

IngredientStrength
TRETINOIN.025 g/100g

Pharmacological Class

  • Retinoid [EPC]
  • Retinoids [CS]
  • Arteriolar Vasodilation [PE]
  • Arteriolar Vasodilator [EPC]
  • Retinoid [EPC]
  • Retinoids [CS]
  • Arteriolar Vasodilation [PE]
  • Arteriolar Vasodilator [EPC]

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.