DEXAMETHASONE SODIUM PHOSPHATE 0.1% / FINASTERIDE 0.1% / MINOXIDIL 5%- dexamethasone sodium phosphate 0.1% / finasteride 0.1% / minoxidil 5% 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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DEXAMETHASONE SODIUM PHOSPHATE 0.1% / FINASTERIDE 0.1% / MINOXIDIL 5%

Directions for use

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Sincerus Florida, LLC. Adverse reactions

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Active, inactive

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NDC 72934-4069-8 DEXAMETHASONE SODIUM PHOSPHATE USP 0.1% / FINASTERIDE USP 0.1% / MINOXIDIL USP 5% . Solution 60 gm

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DEXAMETHASONE SODIUM PHOSPHATE 0.1% / FINASTERIDE 0.1% / MINOXIDIL 5% 
dexamethasone sodium phosphate 0.1% / finasteride 0.1% / minoxidil 5% solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-4069
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 100 g
FINASTERIDE (UNII: 57GNO57U7G) (FINASTERIDE - UNII:57GNO57U7G) FINASTERIDE0.1 g  in 100 g
DEXAMETHASONE SODIUM PHOSPHATE (UNII: AI9376Y64P) (DEXAMETHASONE - UNII:7S5I7G3JQL) DEXAMETHASONE PHOSPHATE0.1 g  in 100 g
Product Characteristics
Colorwhite (off white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-4069-860 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product05/09/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/09/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-4069)

Revised: 5/2019
Document Id: 8861bc75-99f4-44f2-e053-2a95a90a1fe0
Set id: 8861bc75-99f3-44f2-e053-2a95a90a1fe0
Version: 1
Effective Time: 20190508
 
Sincerus Florida, LLC