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.

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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 Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-4147
Route of Administration TOPICAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 7 g  in 100 g
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 4 g  in 100 g
Product Characteristics
Color white (Clear solution) Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:72934-4147-8 60 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/10/2019
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 05/10/2019
Labeler - Sincerus Florida, LLC (080105003)
Establishment
Name Address ID/FEI Business Operations
Sincerus Florida, LLC 080105003 manufacture(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