MINOXIDIL 7% / TRETINOIN 0.025% solution

MINOXIDIL 7% / TRETINOIN 0.025% by

Drug Labeling and Warnings

MINOXIDIL 7% / TRETINOIN 0.025% 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, Adverse reactions

Active, inactive

NDC:

72934-4150-8 MINOXIDIL 7% / TRETINOIN 0.025%. Solution 60 gm.

INGREDIENTS AND APPEARANCE

MINOXIDIL 7% / TRETINOIN 0.025% 
minoxidil 7% / tretinoin 0.025% solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 72934-4150
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R)	TRETINOIN	0.025 g  in 100 g
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL	7 g  in 100 g

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72934-4150-8	60 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	05/07/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/07/2019

Labeler - Sincerus Florida, LLC (080105003)

Establishment
Name	Address	ID/FEI	Business Operations
Sincerus Florida, LLC		080105003	manufacture(72934-4150)