NIACINAMIDE 4% / TRETINOIN 0.1%- niacinamide 4% / tretinoin 0.1% gel
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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NIACINAMIDE 4% / TRETINOIN 0.1% GEL

Directions for use

Directions for use As directed by physician. Apply topically. For external use only. Wash hands after use. Store at controlled room temperature 20-25 Celsius

Sincerus Florida, LLC; Adverse reactions

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Active;Inactive

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NDC 72934-1165-2
NIACINAMIDE 4% / TRETINOIN 0.1% GEL 30gm

Gel 30gm Sincerus Florida This is a compounded drug Made in USA

NIACINAMIDE 4% / TRETINOIN 0.1%
niacinamide 4% / tretinoin 0.1% gel

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:72934-1165
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R)	TRETINOIN	0.1 g in 100 g
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	4 g in 100 g

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72934-1165-2	30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2019

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

Labeler - Sincerus Florida, LLC (080105003)

Name	Address	ID/FEI	Business Operations
Establishment
Sincerus Florida, LLC		080105003	manufacture(72934-1165)

NIACINAMIDE 4% / TRETINOIN 0.1% GEL

Directions for use

Sincerus Florida, LLC; Adverse reactions

Active;Inactive

NDC 72934-1165-2 NIACINAMIDE 4% / TRETINOIN 0.1% GEL 30gm

NDC 72934-1165-2
NIACINAMIDE 4% / TRETINOIN 0.1% GEL 30gm