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

MINOXIDIL 7% / NIACINAMIDE 4% by

Drug Labeling and Warnings

MINOXIDIL 7% / NIACINAMIDE 4% by is a Prescription medication manufactured, distributed, or labeled by Sincerus Florida, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Directions for use

Sincerus Florida, LLC. Adverse reactions

Active, inactive

NDC:

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

INGREDIENTS AND APPEARANCE

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)