FINASTERIDE 0.1% / MINOXIDIL 7%- finasteride 0.1% / minoxidil 7% solution 
Sincerus Florida, LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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FINASTERIDE 0.1% / MINOXIDIL 7%

Directions for Use

c

Sincerus Florida, LLC adverse reactions

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Active, inactive

g

NDC 72934-4075-8 FINASTERIDE USP 0.1% / MINOXIDIL USP 7%. Solution 60gm

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FINASTERIDE 0.1% / MINOXIDIL 7% 
finasteride 0.1% / minoxidil 7% solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-4075
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FINASTERIDE (UNII: 57GNO57U7G) (FINASTERIDE - UNII:57GNO57U7G) FINASTERIDE0.1 g  in 100 g
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL7 g  in 100 g
Product Characteristics
Colorwhite (CLEAR SOLUTION) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-4075-860 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product05/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/01/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-4075)

Revised: 4/2019
Document Id: 8747ab73-38f8-0828-e053-2a95a90a99cd
Set id: 8747ab73-38f7-0828-e053-2a95a90a99cd
Version: 1
Effective Time: 20190424
 
Sincerus Florida, LLC