MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025%- minoxidil 7% / progesterone 0.1% / tretinoin 0.025% 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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MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025%

Directions for use

Sincerus Florida, adverse reactions

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MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025%
minoxidil 7% / progesterone 0.1% / tretinoin 0.025% solution

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y)	PROGESTERONE	0.1 g in 100 g
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL	7 g in 100 g
TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R)	TRETINOIN	0.025 g in 100 g

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72934-4149-8	60 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	05/07/2019

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

Labeler - Sincerus Florida, LLC (080105003)

Name	Address	ID/FEI	Business Operations
Establishment
Sincerus Florida, LLC		080105003	manufacture(72934-4149)