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011312 NIACINAMIDE 4% / TAZAROTENE 0.05%

011312 NIACINAMIDE 4% / TAZAROTENE 0.05%

Approved
Approval ID

a97a190f-1f98-1fb0-e053-2a95a90a6850

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 2, 2020

Manufacturers
FDA

Sincerus Florida, LLC

DUNS: 080105003

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

011312 NIACINAMIDE 4% / TAZAROTENE 0.05%

PRODUCT DETAILS

NDC Product Code72934-2208
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationTOPICAL
Effective DateJuly 2, 2020
Generic Name011312 NIACINAMIDE 4% / TAZAROTENE 0.05%

INGREDIENTS (2)

TAZAROTENEActive
Quantity: 0.05 g in 100 g
Code: 81BDR9Y8PS
Classification: ACTIB
NIACINAMIDEActive
Quantity: 4 g in 100 g
Code: 25X51I8RD4
Classification: ACTIB
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011312 NIACINAMIDE 4% / TAZAROTENE 0.05% - FDA Approval | MedPath