MINOXIDIL 7% / NIACINAMIDE 4% S- minoxidil 7% / niacinamide 4% 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.

----------

MINOXIDIL 7% / NIACINAMIDE 4%

Directions for use

ed

Sincerus Florida, LLC. Adverse reactions

xx

Active, inactive

ca

NDC 72934-4147-8. MINOXIDIL 7% / NIACINAMIDE 4%. Solution 60 gm

sf

MINOXIDIL 7% / NIACINAMIDE 4%  S
minoxidil 7% / niacinamide 4% solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:72934-4147
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL7 g  in 100 g
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE4 g  in 100 g
Product Characteristics
Colorwhite (Clear solution) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72934-4147-860 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/10/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/10/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
NameAddressID/FEIBusiness Operations
Sincerus Florida, LLC080105003manufacture(72934-4147)

Revised: 5/2019
Document Id: 8875a838-5aa4-3407-e053-2a95a90ae3eb
Set id: 8875a838-5aa3-3407-e053-2a95a90ae3eb
Version: 1
Effective Time: 20190509
 
Sincerus Florida, LLC