FLUOCINOLONE ACETONIDE 0.01% / MINOXIDIL 7% / PROGESTERONE 0.1%- fluocinolone acetonide 0.01% / minoxidil 7% / progesterone 0.1% 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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FLUOCINOLONE ACETONIDE 0.01% / MINOXIDIL 7% / PROGESTERONE 0.1%

Directions for use

Sincerus Florida, LLC. Adverse reactions

Active, inactive

NDC 72934-4080-8. FLUOCINOLONE ACETONIDE USP 0.01% / MINOXIDIL USP 7% / PROGESTERONE USP 0.1%. Solution 60 gm.

FLUOCINOLONE ACETONIDE 0.01% / MINOXIDIL 7% / PROGESTERONE 0.1%
fluocinolone acetonide 0.01% / minoxidil 7% / progesterone 0.1% solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:72934-4080
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FLUOCINOLONE ACETONIDE (UNII: 0CD5FD6S2M) (FLUOCINOLONE ACETONIDE - UNII:0CD5FD6S2M)	FLUOCINOLONE ACETONIDE	0.01 g in 100 g
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL	7 g in 100 g
PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y)	PROGESTERONE	0.1 g in 100 g

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72934-4080-8	60 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	05/09/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		05/09/2019

Labeler - Sincerus florida, LLC (080105003)

Name	Address	ID/FEI	Business Operations
Establishment
Sincerus Florida, LLC		080105003	manufacture(72934-4080)