FINASTERIDE 0.1% / MINOXIDIL 7% solution

FINASTERIDE 0.1% / MINOXIDIL 7% by

Drug Labeling and Warnings

FINASTERIDE 0.1% / MINOXIDIL 7% 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:

72934-4075-8 FINASTERIDE USP 0.1% / MINOXIDIL USP 7%. Solution 60gm

INGREDIENTS AND APPEARANCE

FINASTERIDE 0.1% / MINOXIDIL 7% 
finasteride 0.1% / minoxidil 7% solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 72934-4075
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FINASTERIDE (UNII: 57GNO57U7G) (FINASTERIDE - UNII:57GNO57U7G)	FINASTERIDE	0.1 g  in 100 g
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL	7 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: 72934-4075-8	60 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	05/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2019

Labeler - Sincerus Florida, LLC (080105003)

Establishment
Name	Address	ID/FEI	Business Operations
Sincerus Florida, LLC		080105003	manufacture(72934-4075)