DESOXIMETASONE 0.05% / NIACINAMIDE 4% ointment

DESOXIMETASONE 0.05% / NIACINAMIDE 4% by

Drug Labeling and Warnings

DESOXIMETASONE 0.05% / NIACINAMIDE 4% 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- 5069-2 DESOXIMETASONE USP 0.05% / NIACINAMIDE USP 4%. Ointment 30 gm.

INGREDIENTS AND APPEARANCE

DESOXIMETASONE 0.05% / NIACINAMIDE 4% 
desoximetasone 0.05% / niacinamide 4% ointment

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 72934-5069
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	4 g  in 100 g
DESOXIMETASONE (UNII: 4E07GXB7AU) (DESOXIMETASONE - UNII:4E07GXB7AU)	DESOXIMETASONE	0.05 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72934-5069-2	30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/22/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/22/2019

Labeler - Sincerus Florida, LLC (080105003)

Establishment
Name	Address	ID/FEI	Business Operations
Sincerus Florida, LLC		080105003	manufacture(72934-5069)