BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% solution

BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% by

Drug Labeling and Warnings

BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% 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:

72934-4023-8 BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% Solution 60gm

INGREDIENTS AND APPEARANCE

BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% 
betamethasone dipropionate 0.05% / minoxidil 5% solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 72934-4023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL	5 g  in 100 g
BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U) (BETAMETHASONE - UNII:9842X06Q6M)	BETAMETHASONE	0.05 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: 72934-4023-8	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(72934-4023)