FINASTERIDE 0.1% / MINOXIDIL 7% / TRETINOIN 0.025%- finasteride 0.1% / minoxidil 7% / tretinoin 0.025% 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% / TRETINOIN 0.025%

Directions for use

f

Sincerus Florida, LLC . Adverse reactions

a

Active, inactive

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NDC 72934-4076-8 FINASTERIDE USP 0.1% / MINOXIDIL USP 7% / TRETINOIN USP0.025%. Solution 60gm.

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FINASTERIDE 0.1% / MINOXIDIL 7% / TRETINOIN 0.025% 
finasteride 0.1% / minoxidil 7% / tretinoin 0.025% solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-4076
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL7 g  in 100 g
FINASTERIDE (UNII: 57GNO57U7G) (FINASTERIDE - UNII:57GNO57U7G) FINASTERIDE0.1 g  in 100 g
TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN0.025 g  in 100 g
Product Characteristics
ColoryellowScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-4076-860 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product05/11/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/11/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-4076)

Revised: 5/2019
Document Id: 888b7a9c-cf70-7c3a-e053-2a95a90ae214
Set id: 888b7a9c-cf6f-7c3a-e053-2a95a90ae214
Version: 1
Effective Time: 20190510
 
Sincerus Florida, LLC